Высшая валентность элемента определяется номером периода

Валентность — это способность атомов химических элементов образовывать определенное число химических связей с атомами других химических элементов.

Ковалентные связи могут образовываться по обменному и донорно-акцепторному механизмам.

Обменный механизм образования ковалентной связив образовании связи участвуют одноэлектронные атомные орбитали, т.е. каждый из атомов предоставляет по одному неспаренному электрону.

Обменный механизм образования связи

Донорно-акцепторный механизм — образование связи происходит за счет электронной пары одного из атомов (атом-донор) и вакантной орбитали другого атома (атом-акцептор):

Донорно-акцепторный механизм

Таким образом, атомы могут образовывать химическую  связь не только за счет неспаренных электронов на внешнем энергетическом уровне, но и за счет неподеленных электронных пар, или свободных орбиталей на этом уровне.

Большинство элементов характеризуются высшей, низшей или промежуточной валентностью в соединениях. 

Для большинства элементов высшая валентность, как правило, равна номеру группы, низшая валентность определяется по формуле: 8 — № группы. Промежуточная валентность – это число между низшей и высшей валентностями.

Например, высшая валентность хлора равна VII, низшая валентность хлора равна I, промежуточные валентности — III, V.

Обратите внимание! Степень окисления и валентность — это не одно и то же. Хотя иногда степени окисления совпадают с валентностями. Стпень окисления — это условный заряд атома, он может быть и положительным и отрицательным. А вот образовать отрицательное число связей атом никак не может.

Например, валентность (число связей) атома кислорода в молекуле O2 равна II, а вот степень окисления атома кислорода равна 0.

Большинство элементов проявляют переменную валентность в соединениях, но некоторые элементы проявляют постоянную валентность. Их необходимо запомнить:

Элемент Валентность
Фтор F I
Кислород О II
Металлы IA группы  (Li, Na, K, Rb, Cs, Fr) I
Металлы IIA группы (Be, Mg, Ca, Sr, Ba, Ra) II
Алюминий Al III

Как определить валентность атома в соединении?


Рассмотрим валентные возможности атомов второго периода. В силу некоторых ограничений они не соответствуют традиционным «школьным» представлениям.

Итак, не внешнем энергетическом уровне лития 1 неспаренный электрон: 1s22s1.

+3Li 1s2  2s1 

Следовательно, литий может образовывать одну связь и валентность лития I.


У бериллия на внешнем энергетическом уровне 2 электрона: 1s22s2.

+4Be 1s2  2s2 

В возбужденном состоянии возможен переход электронов внешнего энергетического уровня с одного подуровня на другой: 1s22s12p1. 

+4Be* 1s2  2s1  2p1

Таким образом, на внешнем энергетическом уровне бериллия в возбужденном энергетическом состоянии  есть 2 неспаренных электрона и две вакантные электронные орбитали. Следовательно, бериллий может образовать 2 связи по обменному механизму, т.е. валентность бериллия равна номеру группы  и равна II.

Например, в хлориде бериллия валентность бериллия равна II:


Электронная конфигурация атома бора в основном состоянии +5B 1s22s22p1:

+5B 1s2  2s2  2p1

В возбужденном состоянии: +5B* 1s22s12p2.

+5B 1s2  2s1  2p2

Следовательно, бор может образовывать 3 связи по обменному механизму (за счет неспаренных электронов). Валентность бора в соединениях — III.

Например, в трихлориде бора BCl3 валентность бора равна III.

Однако, при этом у бора остается еще одна вакантная электронная орбиталь. Следовательно, бор может выступать, как акцептор электронной пары.

У атома углерода в возбужденном состоянии на внешнем энергетическом уровне 4 неспаренных электрона: 1s22s12p3, следовательно, максимальная валентность углерода равна IV (как правило, в органических соединениях у углерода именно такая валентность). В основном состоянии у атома углерода 2 неспаренных электрона, и валентность II. Однако посмотрим внимательно: у атома углерода в основном состоянии не внешнем энергетическом уровне есть незанятая (вакантная) электронная орбиталь. Следовательно, он может образовывать еще одну связь — по донорно-акцепторному механизму. Таким образом, в некоторых случаях углерод может образовывать три связи (например, молекула угарного газа CO, строение которой мы рассмотрим позднее).

Валентные возможности атома азота определяются также строением его внешнего энергетического уровня. В основном состоянии электронная формула азота: +7N 1s22s22p3.  

За счет 3 неспаренных электронов на p-подуровне азот может образовывать 3 связи по обменному механизму (валентность III), и еще 1 связь азот может образовать по донорно-акцепторному механизму за счет неподеленной электронной пары. Таким образом, максимальная валентность  азота в соединениях — IV. На примере азота можно убедиться, что высшая валентность атома и максимальная степень окисления — разные величины, которые далеко не всегда совпадают. Возбужденное состояние с 5 неспаренными электронами для атома азота не реализуется, т.к. на 2 энергетическом уровне есть только s и p  орбитали.

Основные характеристики атомов химических элементов:

  • заряд ядра;
  • число электронных слоёв;
  • число электронов на внешнем уровне;
  • радиус атома;
  • высшая валентность в соединениях с кислородом;
  • валентность в летучих водородных соединениях;
  • способность отдавать электроны;
  • способность принимать электроны.

Заряд ядра атома химического элемента равен порядковому номеру. Он последовательно возрастает от одного элемента к другому.

Число электронных слоёв равно номеру периода, к которому относится химический элемент.

Другие свойства изменяются периодически.

Число внешних электронов одинаково у элементов одной (A) группы и совпадает с её номером. В периоде увеличивается от (1) до (8).

Высшие валентности химических элементов в соединениях с кислородом, как правило, совпадают с номером группы и в каждом периоде увеличиваются.

Валентности в соединениях с водородом (для неметаллов), наоборот, уменьшаются и равны разности (8) (–) № группы.

Радиусы атомов в каждом периоде уменьшаются, а в группе увеличиваются.

Химические свойства атомов обусловлены их способностью отдавать электроны или их принимать.

Способность атомов отдавать валентные электроны

Чем больше радиус атома, тем слабее удерживаются его внешние электроны. Поэтому способность отдавать электроны усиливается в группах сверху вниз.

В малых периодах с увеличением зарядов ядер радиус атомов уменьшается, а число электронов на внешнем уровне увеличивается. Они всё сильнее притягиваются к ядру и труднее отрываются от атома.

Легче всего отрываются электроны от атомов щелочного металла франция.

Схематически усиление способности отдавать электроны можно изобразить так:

⇓Fr⇐

Способность атомов притягивать электроны

У элементов одной группы эта способность снижается с увеличением числа электронных слоёв.

В периоде с увеличением заряда ядра радиус атома уменьшается, число валентных электронов и их притяжение к ядру растёт, и атомам всё легче присоединять дополнительные электроны на внешний уровень.

Наиболее активно принимают электроны атомы галогена фтора.

Изменение способности принимать электроны показывает схема:

 ⇒F⇑

Отличаются от других элементов по свойствам инертные газы (элементы 

VIIIA

 группы). Их атомы имеют заполненные внешние энергетические уровни и поэтому не отдают и не принимают электроны.

Подведём итоги.

Закономерности изменения свойств атомов

Свойство

 В периоде

 В группе

Заряд ядра

 увеличивается  увеличивается

Радиус атома

 уменьшается  увеличивается

Способность отдавать электроны

 уменьшается  увеличивается

Число валентных электронов

 увеличивается  не изменяется

Способность принимать электроны

 увеличивается  уменьшается

Высшая валентность в оксидах и гидроксидах

 увеличивается  не изменяется

Валентность в летучих водородных соединениях

 уменьшается  не изменяется

Для
стехиометрических расчетов, а также
для составления химических формул и
уравнений необходимо знание количественных
соотношений атомов различных элементов,
в которых они соединяются или
взаимодействуют. Такая информация
передаётся стехиометрической валентностью.
Стехиометрическая
валентность элемента
показывает,
со сколькими атомами одновалентного
элемента соединяется атом данного
элемента.
Примером одновалентного элемента
является водород, поэтому стехиометрическая
валентность указывает на то, со сколькими
атомами водорода соединяется атом
рассматриваемого элемента. Так, в HCl
хлор одновалентен, в H2O
кислород двухвалентен, в NH3
азот трехвалентен и т.д.

Водородные
соединения известны не для всех элементов,
но почти все элементы образуют соединения
с кислородом, который всегда стехиометрически
двухвалентен. Поэтому валентность
элементов можно определять по составу
их кислородных соединений. Например,
калий одновалентен (K2O),
барий двухвалентен (BaO), алюминий
трехвалентен (Al2O3).

Многие
элементы проявляют несколько
стехиометрических валентностей, т.е.
они могут образовывать с другим элементом
несколько соединений разного
стехиометрического состава. Например,
азот в соединениях с кислородом может
быть одновалентным (N2O),
двухвалентным (NO), трехвалентным (N2O3),
четырех-валентным (NO2)
и пятивалентным (N2O5).

Понятие
о стехиометрической валентности было
введено в химию задолго до того, как
стало известно строение атомов (Франкланд,
1853). При изучении строения атомов было
установлено, что валентность элементов
связана с числом внешних электронов в
их атомах.

Для
всех элементов главных подгрупп число
внешних электронов у их атомов равно
номеру группы. Внешние электроны
одновременно являются валентными
электронами, поэтому высшая валентность
элементов главных подгрупп равна номеру
группы. Исключением из этого правила
является кислород, который всегда
двухвалентен, хотя находится в шестой
группе, и фтор, который находится в
седьмой группе, но всегда одновалентен.
В табл. 5 приведены значения максимальной
валентности элементов трех первых
периодов.

Таблица
5. Максимальная валентность элементов
первого, второго и третьего периодов

Элемент

Валентность

Элемент

Валентность

Элемент

Валентность

H

1

Li

1

Na

1

Be

2

Mg

2

B

3

Al

3

C

4

Si

4

N

5

P

5

O

2

S

6

F

1

Cl

7

Максимальная
валентность химических элементов
главных подгрупп является периодическим
свойством (рис. 5в):
в периодах она увеличивается, а в группах
постоянна и равна номеру группы (кроме
кислорода и фтора). Для элементов побочных
подгрупп валентность также является
периодическим свойством, но зависимость
их валентности от положения в периодической
системе является более сложной.

Рис 5. Зависимость
валентности от атомного номера элемента.

Пример
3.
Руководствуясь
положением элементов в периодической
системе, напишите формулы соединения
алюминия с водородом, кислородом, азотом,
углеродом, серой и фтором.

Ответ.
AlH3,
Al2O3,
AlN, Al4C3,
Al2S3,
AlF3

In chemistry, the valence (US spelling) or valency (British spelling) of an element is the measure of its combining capacity with other atoms when it forms chemical compounds or molecules.

Description

The combining capacity, or affinity of an atom of a given element is determined by the number of hydrogen atoms that it combines with. In methane, carbon has a valence of 4; in ammonia, nitrogen has a valence of 3; in water, oxygen has a valence of 2; and in hydrogen chloride, chlorine has a valence of 1. Chlorine, as it has a valence of one, can be substituted for hydrogen. Phosphorus has a valence of 5 in phosphorus pentachloride, PCl5. Valence diagrams of a compound represent the connectivity of the elements, with lines drawn between two elements, sometimes called bonds, representing a saturated valency for each element.[1] The two tables below show some examples of different compounds, their valence diagrams, and the valences for each element of the compound.

Compound H2
Hydrogen
CH4
Methane
C3H8
Propane
C3H6
Propylene
C2H2
Acetylene
Diagram Wasserstoff.svg Methane-2D-flat-small.png Propane-2D-flat.png Propene-2D-flat.svg Ethyne-2D-flat.png
Valencies
  • Hydrogen: 1
  • Carbon: 4
  • Hydrogen: 1
  • Carbon: 4
  • Hydrogen: 1
  • Carbon: 4
  • Hydrogen: 1
  • Carbon: 4
  • Hydrogen: 1
Compound NH3
Ammonia
NaCN
Sodium cyanide
PSCl3
Thiophosphoryl chloride
H2S
Hydrogen sulfide
H2SO4
Sulfuric acid
H2S2O6
Dithionic acid
Cl2O7
Dichlorine heptoxide
XeO4
Xenon tetroxide
Diagram Ammoniak.png Sodium cyanide-2D.svg Thiophosphoryl-chloride-2D.png Hydrogen sulfide.svg Sulfuric acid chemical structure.png Dithionic-acid-2D.png Dichlorine heptoxide.svg Xenon-tetroxide-2D.png
Valencies
  • Nitrogen: 3
  • Hydrogen: 1
  • Sodium: 1
  • Carbon: 4
  • Nitrogen: 3
  • Phosphorus: 5
  • Sulfur: 2
  • Chlorine: 1
  • Sulfur: 2
  • Hydrogen: 1
  • Sulfur: 6
  • Oxygen: 2
  • Hydrogen: 1
  • Sulfur: 6
  • Oxygen: 2
  • Hydrogen: 1
  • Chlorine: 7
  • Oxygen: 2
  • Xenon: 8
  • Oxygen: 2

Modern definitions

Valence is defined by the IUPAC as:[2]

The maximum number of univalent atoms (originally hydrogen or chlorine atoms) that may combine with an atom of the element under consideration, or with a fragment, or for which an atom of this element can be substituted.

An alternative modern description is:[3]

The number of hydrogen atoms that can combine with an element in a binary hydride or twice the number of oxygen atoms combining with an element in its oxide or oxides.

This definition differs from the IUPAC definition as an element can be said to have more than one valence.

A very similar modern definition given in a recent article defines the valence of a particular atom in a molecule as «the number of electrons that an atom uses in bonding», with two equivalent formulas for calculating valence:[4]

valence = number of electrons in valence shell of free atomnumber of non-bonding electrons on atom in molecule,

and

valence = number of bonds + formal charge.

Historical development

The etymology of the words valence (plural valences) and valency (plural valencies) traces back to 1425, meaning «extract, preparation», from Latin valentia «strength, capacity», from the earlier valor «worth, value», and the chemical meaning referring to the «combining power of an element» is recorded from 1884, from German Valenz.[5]

The concept of valence was developed in the second half of the 19th century and helped successfully explain the molecular structure of inorganic and organic compounds.[1]
The quest for the underlying causes of valence led to the modern theories of chemical bonding, including the cubical atom (1902), Lewis structures (1916), valence bond theory (1927), molecular orbitals (1928), valence shell electron pair repulsion theory (1958), and all of the advanced methods of quantum chemistry.

In 1789, William Higgins published views on what he called combinations of «ultimate» particles, which foreshadowed the concept of valency bonds.[6] If, for example, according to Higgins, the force between the ultimate particle of oxygen and the ultimate particle of nitrogen were 6, then the strength of the force would be divided accordingly, and likewise for the other combinations of ultimate particles (see illustration).

The exact inception, however, of the theory of chemical valencies can be traced to an 1852 paper by Edward Frankland, in which he combined the older radical theory with thoughts on chemical affinity to show that certain elements have the tendency to combine with other elements to form compounds containing 3, i.e., in the 3-atom groups (e.g., NO3, NH3, NI3, etc.) or 5, i.e., in the 5-atom groups (e.g., NO5, NH4O, PO5, etc.), equivalents of the attached elements. According to him, this is the manner in which their affinities are best satisfied, and by following these examples and postulates, he declares how obvious it is that[7]

A tendency or law prevails (here), and that, no matter what the characters of the uniting atoms may be, the combining power of the attracting element, if I may be allowed the term, is always satisfied by the same number of these atoms.

This “combining power” was afterwards called quantivalence or valency (and valence by American chemists).[6] In 1857 August Kekulé proposed fixed valences for many elements, such as 4 for carbon, and used them to propose structural formulas for many organic molecules, which are still accepted today.

Most 19th-century chemists defined the valence of an element as the number of its bonds without distinguishing different types of valence or of bond. However, in 1893 Alfred Werner described transition metal coordination complexes such as [Co(NH3)6]Cl3, in which he distinguished principal and subsidiary valences (German: ‘Hauptvalenz’ and ‘Nebenvalenz’), corresponding to the modern concepts of oxidation state and coordination number respectively.

For main-group elements, in 1904 Richard Abegg considered positive and negative valences (maximal and minimal oxidation states), and proposed Abegg’s rule to the effect that their difference is often 8.

Electrons and valence

The Rutherford model of the nuclear atom (1911) showed that the exterior of an atom is occupied by electrons, which suggests that electrons are responsible for the interaction of atoms and the formation of chemical bonds. In 1916, Gilbert N. Lewis explained valence and chemical bonding in terms of a tendency of (main-group) atoms to achieve a stable octet of 8 valence-shell electrons. According to Lewis, covalent bonding leads to octets by the sharing of electrons, and ionic bonding leads to octets by the transfer of electrons from one atom to the other. The term covalence is attributed to Irving Langmuir, who stated in 1919 that «the number of pairs of electrons which any given atom shares with the adjacent atoms is called the covalence of that atom».[8] The prefix co- means «together», so that a co-valent bond means that the atoms share a valence. Subsequent to that, it is now more common to speak of covalent bonds rather than valence, which has fallen out of use in higher-level work from the advances in the theory of chemical bonding, but it is still widely used in elementary studies, where it provides a heuristic introduction to the subject.

In the 1930s, Linus Pauling proposed that there are also polar covalent bonds, which are intermediate between covalent and ionic, and that the degree of ionic character depends on the difference of electronegativity of the two bonded atoms.

Pauling also considered hypervalent molecules, in which main-group elements have apparent valences greater than the maximal of 4 allowed by the octet rule. For example, in the sulfur hexafluoride molecule (SF6), Pauling considered that the sulfur forms 6 true two-electron bonds using sp3d2 hybrid atomic orbitals, which combine one s, three p and two d orbitals. However more recently, quantum-mechanical calculations on this and similar molecules have shown that the role of d orbitals in the bonding is minimal, and that the SF6 molecule should be described as having 6 polar covalent (partly ionic) bonds made from only four orbitals on sulfur (one s and three p) in accordance with the octet rule, together with six orbitals on the fluorines.[9] Similar calculations on transition-metal molecules show that the role of p orbitals is minor, so that one s and five d orbitals on the metal are sufficient to describe the bonding.[10]

Common valences

For elements in the main groups of the periodic table, the valence can vary between 1 and 7.

Group Valence 1 Valence 2 Valence 3 Valence 4 Valence 5 Valence 6 Valence 7 Valence 8 Typical valences
1 (I) NaCl 1
2 (II) MgCl2 2
13 (III) BCl3
AlCl3
Al2O3
3
14 (IV) CO CH4 4
15 (V) NO NH3
PH3
As2O3
NO2 N2O5
PCl5
3 and 5
16 (VI) H2O
H2S
SO2 SO3 2 and 6
17 (VII) HCl HClO2 ClO2 HClO3 Cl2O7 1 and 7
18 (VIII) XeO4 8

Many elements have a common valence related to their position in the periodic table, and nowadays this is rationalised by the octet rule.
The Greek/Latin numeral prefixes (mono-/uni-, di-/bi-, tri-/ter-, and so on) are used to describe ions in the charge states 1, 2, 3, and so on, respectively. Polyvalence or multivalence refers to species that are not restricted to a specific number of valence bonds. Species with a single charge are univalent (monovalent). For example, the Cs+ cation is a univalent or monovalent cation, whereas the Ca2+ cation is a divalent cation, and the Fe3+ cation is a trivalent cation. Unlike Cs and Ca, Fe can also exist in other charge states, notably 2+ and 4+, and is thus known as a multivalent (polyvalent) ion.[11] Transition metals and metals to the right are typically multivalent but there is no simple pattern predicting their valency.[12]

Valence adjectives using the -valent suffix†

Valence More common adjective‡ Less common synonymous adjective‡§
0-valent zerovalent nonvalent
1-valent monovalent univalent
2-valent divalent bivalent
3-valent trivalent tervalent
4-valent tetravalent quadrivalent
5-valent pentavalent quinquevalent, quinquivalent
6-valent hexavalent sexivalent
7-valent heptavalent septivalent
8-valent octavalent
9-valent nonavalent
10-valent decavalent
12-valent dodecavalent
multiple / many / variable polyvalent multivalent
together covalent
not together noncovalent

† The same adjectives are also used in medicine to refer to vaccine valence, with the slight difference that in the latter sense, quadri- is more common than tetra-.

‡ As demonstrated by hit counts in Google web search and Google Books search corpora (accessed 2017).

§ A few other forms can be found in large English-language corpora (for example, *quintavalent, *quintivalent, *decivalent), but they are not the conventionally established forms in English and thus are not entered in major dictionaries.

Valence versus oxidation state

Because of the ambiguity of the term valence,[13] other notations are currently preferred. Beside the system of oxidation states (also called oxidation numbers) as used in Stock nomenclature for coordination compounds,[14] and the lambda notation, as used in the IUPAC nomenclature of inorganic chemistry,[15] oxidation state is a more clear indication of the electronic state of atoms in a molecule.

The oxidation state of an atom in a molecule gives the number of valence electrons it has gained or lost.[16] In contrast to the valency number, the oxidation state can be positive (for an electropositive atom) or negative (for an electronegative atom).

Elements in a high oxidation state have an oxidation state higher than +4, and also, elements in a high valence state (hypervalent elements) have a valence higher than 4. For example, in perchlorates ClO4, chlorine has 7 valence bonds (thus, it is heptavalent, in other words, it has valence 7), and it has oxidation state +7; in ruthenium tetroxide RuO4, ruthenium has 8 valence bonds (thus, it is octavalent, in other words, it has valence 8), and it has oxidation state +8.

In some scenarios, the difference between valence and oxidation state arises. Valence and oxidation state of the same atom may not be the same. For example, in disulfur decafluoride molecule S2F10, each sulfur atom has 6 valence bonds (5 single bonds with fluorine atoms and 1 single bond with sulfur atom), thus, each sulfur atom is hexavalent, in other words, it has valence 6, but has oxidation state +5. In dioxygen molecule O2, each oxygen atom has 2 valence bonds, thus, each oxygen atom is divalent, in other words, it has valence 2, but has oxidation state 0. In acetylene H−C≡C−H, each carbon atom has 4 valence bonds (1 single bond with hydrogen atom and 3 single bonds with carbon atom), thus, each carbon atom is tetravalent, in other words, it has valence 4, but has oxidation state −1.

Examples

Variation of valence vs oxidation state for bonds between two different elements

Compound Formula Valence Oxidation state Diagram
Hydrogen chloride HCl H = 1   Cl = 1 H = +1   Cl = −1 H−Cl
Perchloric acid * HClO4 H = 1   Cl = 7   O = 2 H = +1   Cl = +7   O = −2 Perchloric acid molecule diagram.png
Methane CH4 C = 4   H = 1 C = −4   H = +1 Methane molecule diagram.png
Dichloromethane ** CH2Cl2 C = 4   H = 1   Cl = 1 C = 0   H = +1   Cl = −1 Dichloromethane molecular structure.svg
Ferrous oxide *** FeO Fe = 2   O = 2 Fe = +2   O = −2 Fe=O
Ferric oxide *** Fe2O3 Fe = 3   O = 2 Fe = +3   O = −2 O=Fe−O−Fe=O
Sodium hydride NaH Na = 1   H = 1 Na = +1   H = −1 Na−H

* The perchlorate ion ClO4 is monovalent, in other words, it has valence 1.
** Valences may also be different from absolute values of oxidation states due to different polarity of bonds. For example, in dichloromethane, CH2Cl2, carbon has valence 4 but oxidation state 0.
*** Iron oxides appear in a crystal structure, so no typical molecule can be identified. In ferrous oxide, Fe has oxidation state +2; in ferric oxide, oxidation state +3.

Variation of valence vs oxidation state for bonds between two atoms of the same element

Compound Formula Valence Oxidation state Diagram
Hydrogen H2 H = 1 H = 0 H−H
Chlorine Cl2 Cl = 1 Cl = 0 Cl−Cl
Hydrogen peroxide H2O2 H = 1   O = 2 H = +1   O = −1 Wasserstoffperoxid.svg
Hydrazine N2H4 H = 1   N = 3 H = +1   N = −2 Hydrazine-2D-A1.png
Disulfur decafluoride S2F10 S = 6   F = 1 S = +5   F = −1 Disulfur-decafluoride-diagram.png
Dithionic acid H2S2O6 S = 6   O = 2   H = 1 S = +5   O = −2   H = +1 Dithionic-acid-2D.png
Hexachloroethane C2Cl6 C = 4   Cl = 1 C = +3   Cl = −1 Hexachloroethane-2D-stereo.png
Ethylene C2H4 C = 4   H = 1 C = −2   H = +1 Ethylene molecule diagram.png
Acetylene C2H2 C = 4   H = 1 C = −1   H = +1 H−C≡C−H
Mercury(I) chloride Hg2Cl2 Hg = 2   Cl = 1 Hg = +1   Cl = −1 Cl−Hg−Hg−Cl

«Maximum number of bonds» definition

Frankland took the view that the valence (he used the term «atomicity») of an element was a single value that corresponded to the maximum value observed. The number of unused valencies on atoms of what are now called the p-block elements is generally even, and Frankland suggested that the unused valencies saturated one another. For example, nitrogen has a maximum valence of 5, in forming ammonia two valencies are left unattached; sulfur has a maximum valence of 6, in forming hydrogen sulphide four valencies are left unattached.[17][18]

The International Union of Pure and Applied Chemistry (IUPAC) has made several attempts to arrive at an unambiguous definition of valence. The current version, adopted in 1994:[19]

The maximum number of univalent atoms (originally hydrogen or chlorine atoms) that may combine with an atom of the element under consideration, or with a fragment, or for which an atom of this element can be substituted.[2]

Hydrogen and chlorine were originally used as examples of univalent atoms, because of their nature to form only one single bond. Hydrogen has only one valence electron and can form only one bond with an atom that has an incomplete outer shell. Chlorine has seven valence electrons and can form only one bond with an atom that donates a valence electron to complete chlorine’s outer shell. However, chlorine can also have oxidation states from +1 to +7 and can form more than one bond by donating valence electrons.

Hydrogen has only one valence electron, but it can form bonds with more than one atom. In the bifluoride ion ([HF2]), for example, it forms a three-center four-electron bond with two fluoride atoms:

[F−H F ↔ F H−F]

Another example is the three-center two-electron bond in diborane (B2H6).

Maximum valences of the elements

Maximum valences for the elements are based on the data from list of oxidation states of the elements. They are shown by the color code at the bottom of the table.

  • v
  • t
  • e

Maximum valences of the elements

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18
Group →
↓ Period
1 1
H
2
He
2 3
Li
4
Be
5
B
6
C
7
N
8
O
9
F
10
Ne
3 11
Na
12
Mg
13
Al
14
Si
15
P
16
S
17
Cl
18
Ar
4 19
K
20
Ca
21
Sc
22
Ti
23
V
24
Cr
25
Mn
26
Fe
27
Co
28
Ni
29
Cu
30
Zn
31
Ga
32
Ge
33
As
34
Se
35
Br
36
Kr
5 37
Rb
38
Sr
39
Y
40
Zr
41
Nb
42
Mo
43
Tc
44
Ru
45
Rh
46
Pd
47
Ag
48
Cd
49
In
50
Sn
51
Sb
52
Te
53
I
54
Xe
6 55
Cs
56
Ba
1 asterisk 71
Lu
72
Hf
73
Ta
74
W
75
Re
76
Os
77
Ir
78
Pt
79
Au
80
Hg
81
Tl
82
Pb
83
Bi
84
Po
85
At
86
Rn
7 87
Fr
88
Ra
1 asterisk 103
Lr
104
Rf
105
Db
106
Sg
107
Bh
108
Hs
109
Mt
110
Ds
111
Rg
112
Cn
113
Nh
114
Fl
115
Mc
116
Lv
117
Ts
118
Og
 
1 asterisk 57
La
58
Ce
59
Pr
60
Nd
61
Pm
62
Sm
63
Eu
64
Gd
65
Tb
66
Dy
67
Ho
68
Er
69
Tm
70
Yb
1 asterisk 89
Ac
90
Th
91
Pa
92
U
93
Np
94
Pu
95
Am
96
Cm
97
Bk
98
Cf
99
Es
100
Fm
101
Md
102
No
Maximum valences are based on the List of oxidation states of the elements


0
1
2
3
4
5
6
7
8
9
Unknown
Background color shows maximum valence of the chemical element

Primordial From decay SyntheticBorder shows natural occurrence of the element

See also

  • Abegg’s rule
  • Oxidation state

References

  1. ^ a b Partington, James Riddick (1921). A text-book of inorganic chemistry for university students (1st ed.). OL 7221486M.
  2. ^ a b IUPAC Gold Book definition: valence
  3. ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
  4. ^ Parkin, Gerard (May 2006). «Valence, Oxidation Number, and Formal Charge: Three Related but Fundamentally Different Concepts». Journal of Chemical Education. 83 (5): 791. doi:10.1021/ed083p791. ISSN 0021-9584.
  5. ^ Harper, Douglas. «valence». Online Etymology Dictionary.
  6. ^ a b Partington, J.R. (1989). A Short History of Chemistry. Dover Publications, Inc. ISBN 0-486-65977-1.
  7. ^ Frankland, E. (1852). «On a New Series of Organic Bodies Containing Metals». Philosophical Transactions of the Royal Society of London. 142: 417–444. doi:10.1098/rstl.1852.0020. S2CID 186210604.
  8. ^ Langmuir, Irving (1919). «The Arrangement of Electrons in Atoms and Molecules». Journal of the American Chemical Society. 41 (6): 868–934. doi:10.1021/ja02227a002.
  9. ^ Magnusson, Eric (1990). «Hypercoordinate molecules of second-row elements: d functions or d orbitals?». J. Am. Chem. Soc. 112 (22): 7940–7951. doi:10.1021/ja00178a014.
  10. ^ Frenking, Gernot; Shaik, Sason, eds. (May 2014). «Chapter 7: Chemical bonding in Transition Metal Compounds». The Chemical Bond: Chemical Bonding Across the Periodic Table. Wiley – VCH. ISBN 978-3-527-33315-8.
  11. ^ Merriam-Webster, Merriam-Webster’s Unabridged Dictionary, Merriam-Webster, archived from the original on 2020-05-25, retrieved 2017-05-11.
  12. ^ «Lesson 7: Ions and Their Names». Clackamas Community College. Archived from the original on 21 January 2019. Retrieved 5 February 2019.
  13. ^ The Free Dictionary: valence
  14. ^ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the «Gold Book») (1997). Online corrected version: (2006–) «Oxidation number». doi:10.1351/goldbook.O04363
  15. ^ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the «Gold Book») (1997). Online corrected version: (2006–) «Lambda». doi:10.1351/goldbook.L03418
  16. ^ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the «Gold Book») (1997). Online corrected version: (2006–) «Oxidation state». doi:10.1351/goldbook.O04365
  17. ^ Frankland, E. (1870). Lecture notes for chemical students(Google eBook) (2d ed.). J. Van Voorst. p. 21.
  18. ^ Frankland, E.; Japp, F.R (1885). Inorganic chemistry (1st ed.). pp. 75–85. OL 6994182M.
  19. ^ Muller, P. (1994). «Glossary of terms used in physical organic chemistry (IUPAC Recommendations 1994)». Pure and Applied Chemistry. 66 (5): 1077–1184. doi:10.1351/pac199466051077. S2CID 195819485.

In chemistry, the valence (US spelling) or valency (British spelling) of an element is the measure of its combining capacity with other atoms when it forms chemical compounds or molecules.

Description

The combining capacity, or affinity of an atom of a given element is determined by the number of hydrogen atoms that it combines with. In methane, carbon has a valence of 4; in ammonia, nitrogen has a valence of 3; in water, oxygen has a valence of 2; and in hydrogen chloride, chlorine has a valence of 1. Chlorine, as it has a valence of one, can be substituted for hydrogen. Phosphorus has a valence of 5 in phosphorus pentachloride, PCl5. Valence diagrams of a compound represent the connectivity of the elements, with lines drawn between two elements, sometimes called bonds, representing a saturated valency for each element.[1] The two tables below show some examples of different compounds, their valence diagrams, and the valences for each element of the compound.

Compound H2
Hydrogen
CH4
Methane
C3H8
Propane
C3H6
Propylene
C2H2
Acetylene
Diagram Wasserstoff.svg Methane-2D-flat-small.png Propane-2D-flat.png Propene-2D-flat.svg Ethyne-2D-flat.png
Valencies
  • Hydrogen: 1
  • Carbon: 4
  • Hydrogen: 1
  • Carbon: 4
  • Hydrogen: 1
  • Carbon: 4
  • Hydrogen: 1
  • Carbon: 4
  • Hydrogen: 1
Compound NH3
Ammonia
NaCN
Sodium cyanide
PSCl3
Thiophosphoryl chloride
H2S
Hydrogen sulfide
H2SO4
Sulfuric acid
H2S2O6
Dithionic acid
Cl2O7
Dichlorine heptoxide
XeO4
Xenon tetroxide
Diagram Ammoniak.png Sodium cyanide-2D.svg Thiophosphoryl-chloride-2D.png Hydrogen sulfide.svg Sulfuric acid chemical structure.png Dithionic-acid-2D.png Dichlorine heptoxide.svg Xenon-tetroxide-2D.png
Valencies
  • Nitrogen: 3
  • Hydrogen: 1
  • Sodium: 1
  • Carbon: 4
  • Nitrogen: 3
  • Phosphorus: 5
  • Sulfur: 2
  • Chlorine: 1
  • Sulfur: 2
  • Hydrogen: 1
  • Sulfur: 6
  • Oxygen: 2
  • Hydrogen: 1
  • Sulfur: 6
  • Oxygen: 2
  • Hydrogen: 1
  • Chlorine: 7
  • Oxygen: 2
  • Xenon: 8
  • Oxygen: 2

Modern definitions

Valence is defined by the IUPAC as:[2]

The maximum number of univalent atoms (originally hydrogen or chlorine atoms) that may combine with an atom of the element under consideration, or with a fragment, or for which an atom of this element can be substituted.

An alternative modern description is:[3]

The number of hydrogen atoms that can combine with an element in a binary hydride or twice the number of oxygen atoms combining with an element in its oxide or oxides.

This definition differs from the IUPAC definition as an element can be said to have more than one valence.

A very similar modern definition given in a recent article defines the valence of a particular atom in a molecule as «the number of electrons that an atom uses in bonding», with two equivalent formulas for calculating valence:[4]

valence = number of electrons in valence shell of free atomnumber of non-bonding electrons on atom in molecule,

and

valence = number of bonds + formal charge.

Historical development

The etymology of the words valence (plural valences) and valency (plural valencies) traces back to 1425, meaning «extract, preparation», from Latin valentia «strength, capacity», from the earlier valor «worth, value», and the chemical meaning referring to the «combining power of an element» is recorded from 1884, from German Valenz.[5]

The concept of valence was developed in the second half of the 19th century and helped successfully explain the molecular structure of inorganic and organic compounds.[1]
The quest for the underlying causes of valence led to the modern theories of chemical bonding, including the cubical atom (1902), Lewis structures (1916), valence bond theory (1927), molecular orbitals (1928), valence shell electron pair repulsion theory (1958), and all of the advanced methods of quantum chemistry.

In 1789, William Higgins published views on what he called combinations of «ultimate» particles, which foreshadowed the concept of valency bonds.[6] If, for example, according to Higgins, the force between the ultimate particle of oxygen and the ultimate particle of nitrogen were 6, then the strength of the force would be divided accordingly, and likewise for the other combinations of ultimate particles (see illustration).

The exact inception, however, of the theory of chemical valencies can be traced to an 1852 paper by Edward Frankland, in which he combined the older radical theory with thoughts on chemical affinity to show that certain elements have the tendency to combine with other elements to form compounds containing 3, i.e., in the 3-atom groups (e.g., NO3, NH3, NI3, etc.) or 5, i.e., in the 5-atom groups (e.g., NO5, NH4O, PO5, etc.), equivalents of the attached elements. According to him, this is the manner in which their affinities are best satisfied, and by following these examples and postulates, he declares how obvious it is that[7]

A tendency or law prevails (here), and that, no matter what the characters of the uniting atoms may be, the combining power of the attracting element, if I may be allowed the term, is always satisfied by the same number of these atoms.

This “combining power” was afterwards called quantivalence or valency (and valence by American chemists).[6] In 1857 August Kekulé proposed fixed valences for many elements, such as 4 for carbon, and used them to propose structural formulas for many organic molecules, which are still accepted today.

Most 19th-century chemists defined the valence of an element as the number of its bonds without distinguishing different types of valence or of bond. However, in 1893 Alfred Werner described transition metal coordination complexes such as [Co(NH3)6]Cl3, in which he distinguished principal and subsidiary valences (German: ‘Hauptvalenz’ and ‘Nebenvalenz’), corresponding to the modern concepts of oxidation state and coordination number respectively.

For main-group elements, in 1904 Richard Abegg considered positive and negative valences (maximal and minimal oxidation states), and proposed Abegg’s rule to the effect that their difference is often 8.

Electrons and valence

The Rutherford model of the nuclear atom (1911) showed that the exterior of an atom is occupied by electrons, which suggests that electrons are responsible for the interaction of atoms and the formation of chemical bonds. In 1916, Gilbert N. Lewis explained valence and chemical bonding in terms of a tendency of (main-group) atoms to achieve a stable octet of 8 valence-shell electrons. According to Lewis, covalent bonding leads to octets by the sharing of electrons, and ionic bonding leads to octets by the transfer of electrons from one atom to the other. The term covalence is attributed to Irving Langmuir, who stated in 1919 that «the number of pairs of electrons which any given atom shares with the adjacent atoms is called the covalence of that atom».[8] The prefix co- means «together», so that a co-valent bond means that the atoms share a valence. Subsequent to that, it is now more common to speak of covalent bonds rather than valence, which has fallen out of use in higher-level work from the advances in the theory of chemical bonding, but it is still widely used in elementary studies, where it provides a heuristic introduction to the subject.

In the 1930s, Linus Pauling proposed that there are also polar covalent bonds, which are intermediate between covalent and ionic, and that the degree of ionic character depends on the difference of electronegativity of the two bonded atoms.

Pauling also considered hypervalent molecules, in which main-group elements have apparent valences greater than the maximal of 4 allowed by the octet rule. For example, in the sulfur hexafluoride molecule (SF6), Pauling considered that the sulfur forms 6 true two-electron bonds using sp3d2 hybrid atomic orbitals, which combine one s, three p and two d orbitals. However more recently, quantum-mechanical calculations on this and similar molecules have shown that the role of d orbitals in the bonding is minimal, and that the SF6 molecule should be described as having 6 polar covalent (partly ionic) bonds made from only four orbitals on sulfur (one s and three p) in accordance with the octet rule, together with six orbitals on the fluorines.[9] Similar calculations on transition-metal molecules show that the role of p orbitals is minor, so that one s and five d orbitals on the metal are sufficient to describe the bonding.[10]

Common valences

For elements in the main groups of the periodic table, the valence can vary between 1 and 7.

Group Valence 1 Valence 2 Valence 3 Valence 4 Valence 5 Valence 6 Valence 7 Valence 8 Typical valences
1 (I) NaCl 1
2 (II) MgCl2 2
13 (III) BCl3
AlCl3
Al2O3
3
14 (IV) CO CH4 4
15 (V) NO NH3
PH3
As2O3
NO2 N2O5
PCl5
3 and 5
16 (VI) H2O
H2S
SO2 SO3 2 and 6
17 (VII) HCl HClO2 ClO2 HClO3 Cl2O7 1 and 7
18 (VIII) XeO4 8

Many elements have a common valence related to their position in the periodic table, and nowadays this is rationalised by the octet rule.
The Greek/Latin numeral prefixes (mono-/uni-, di-/bi-, tri-/ter-, and so on) are used to describe ions in the charge states 1, 2, 3, and so on, respectively. Polyvalence or multivalence refers to species that are not restricted to a specific number of valence bonds. Species with a single charge are univalent (monovalent). For example, the Cs+ cation is a univalent or monovalent cation, whereas the Ca2+ cation is a divalent cation, and the Fe3+ cation is a trivalent cation. Unlike Cs and Ca, Fe can also exist in other charge states, notably 2+ and 4+, and is thus known as a multivalent (polyvalent) ion.[11] Transition metals and metals to the right are typically multivalent but there is no simple pattern predicting their valency.[12]

Valence adjectives using the -valent suffix†

Valence More common adjective‡ Less common synonymous adjective‡§
0-valent zerovalent nonvalent
1-valent monovalent univalent
2-valent divalent bivalent
3-valent trivalent tervalent
4-valent tetravalent quadrivalent
5-valent pentavalent quinquevalent, quinquivalent
6-valent hexavalent sexivalent
7-valent heptavalent septivalent
8-valent octavalent
9-valent nonavalent
10-valent decavalent
12-valent dodecavalent
multiple / many / variable polyvalent multivalent
together covalent
not together noncovalent

† The same adjectives are also used in medicine to refer to vaccine valence, with the slight difference that in the latter sense, quadri- is more common than tetra-.

‡ As demonstrated by hit counts in Google web search and Google Books search corpora (accessed 2017).

§ A few other forms can be found in large English-language corpora (for example, *quintavalent, *quintivalent, *decivalent), but they are not the conventionally established forms in English and thus are not entered in major dictionaries.

Valence versus oxidation state

Because of the ambiguity of the term valence,[13] other notations are currently preferred. Beside the system of oxidation states (also called oxidation numbers) as used in Stock nomenclature for coordination compounds,[14] and the lambda notation, as used in the IUPAC nomenclature of inorganic chemistry,[15] oxidation state is a more clear indication of the electronic state of atoms in a molecule.

The oxidation state of an atom in a molecule gives the number of valence electrons it has gained or lost.[16] In contrast to the valency number, the oxidation state can be positive (for an electropositive atom) or negative (for an electronegative atom).

Elements in a high oxidation state have an oxidation state higher than +4, and also, elements in a high valence state (hypervalent elements) have a valence higher than 4. For example, in perchlorates ClO4, chlorine has 7 valence bonds (thus, it is heptavalent, in other words, it has valence 7), and it has oxidation state +7; in ruthenium tetroxide RuO4, ruthenium has 8 valence bonds (thus, it is octavalent, in other words, it has valence 8), and it has oxidation state +8.

In some scenarios, the difference between valence and oxidation state arises. Valence and oxidation state of the same atom may not be the same. For example, in disulfur decafluoride molecule S2F10, each sulfur atom has 6 valence bonds (5 single bonds with fluorine atoms and 1 single bond with sulfur atom), thus, each sulfur atom is hexavalent, in other words, it has valence 6, but has oxidation state +5. In dioxygen molecule O2, each oxygen atom has 2 valence bonds, thus, each oxygen atom is divalent, in other words, it has valence 2, but has oxidation state 0. In acetylene H−C≡C−H, each carbon atom has 4 valence bonds (1 single bond with hydrogen atom and 3 single bonds with carbon atom), thus, each carbon atom is tetravalent, in other words, it has valence 4, but has oxidation state −1.

Examples

Variation of valence vs oxidation state for bonds between two different elements

Compound Formula Valence Oxidation state Diagram
Hydrogen chloride HCl H = 1   Cl = 1 H = +1   Cl = −1 H−Cl
Perchloric acid * HClO4 H = 1   Cl = 7   O = 2 H = +1   Cl = +7   O = −2 Perchloric acid molecule diagram.png
Methane CH4 C = 4   H = 1 C = −4   H = +1 Methane molecule diagram.png
Dichloromethane ** CH2Cl2 C = 4   H = 1   Cl = 1 C = 0   H = +1   Cl = −1 Dichloromethane molecular structure.svg
Ferrous oxide *** FeO Fe = 2   O = 2 Fe = +2   O = −2 Fe=O
Ferric oxide *** Fe2O3 Fe = 3   O = 2 Fe = +3   O = −2 O=Fe−O−Fe=O
Sodium hydride NaH Na = 1   H = 1 Na = +1   H = −1 Na−H

* The perchlorate ion ClO4 is monovalent, in other words, it has valence 1.
** Valences may also be different from absolute values of oxidation states due to different polarity of bonds. For example, in dichloromethane, CH2Cl2, carbon has valence 4 but oxidation state 0.
*** Iron oxides appear in a crystal structure, so no typical molecule can be identified. In ferrous oxide, Fe has oxidation state +2; in ferric oxide, oxidation state +3.

Variation of valence vs oxidation state for bonds between two atoms of the same element

Compound Formula Valence Oxidation state Diagram
Hydrogen H2 H = 1 H = 0 H−H
Chlorine Cl2 Cl = 1 Cl = 0 Cl−Cl
Hydrogen peroxide H2O2 H = 1   O = 2 H = +1   O = −1 Wasserstoffperoxid.svg
Hydrazine N2H4 H = 1   N = 3 H = +1   N = −2 Hydrazine-2D-A1.png
Disulfur decafluoride S2F10 S = 6   F = 1 S = +5   F = −1 Disulfur-decafluoride-diagram.png
Dithionic acid H2S2O6 S = 6   O = 2   H = 1 S = +5   O = −2   H = +1 Dithionic-acid-2D.png
Hexachloroethane C2Cl6 C = 4   Cl = 1 C = +3   Cl = −1 Hexachloroethane-2D-stereo.png
Ethylene C2H4 C = 4   H = 1 C = −2   H = +1 Ethylene molecule diagram.png
Acetylene C2H2 C = 4   H = 1 C = −1   H = +1 H−C≡C−H
Mercury(I) chloride Hg2Cl2 Hg = 2   Cl = 1 Hg = +1   Cl = −1 Cl−Hg−Hg−Cl

«Maximum number of bonds» definition

Frankland took the view that the valence (he used the term «atomicity») of an element was a single value that corresponded to the maximum value observed. The number of unused valencies on atoms of what are now called the p-block elements is generally even, and Frankland suggested that the unused valencies saturated one another. For example, nitrogen has a maximum valence of 5, in forming ammonia two valencies are left unattached; sulfur has a maximum valence of 6, in forming hydrogen sulphide four valencies are left unattached.[17][18]

The International Union of Pure and Applied Chemistry (IUPAC) has made several attempts to arrive at an unambiguous definition of valence. The current version, adopted in 1994:[19]

The maximum number of univalent atoms (originally hydrogen or chlorine atoms) that may combine with an atom of the element under consideration, or with a fragment, or for which an atom of this element can be substituted.[2]

Hydrogen and chlorine were originally used as examples of univalent atoms, because of their nature to form only one single bond. Hydrogen has only one valence electron and can form only one bond with an atom that has an incomplete outer shell. Chlorine has seven valence electrons and can form only one bond with an atom that donates a valence electron to complete chlorine’s outer shell. However, chlorine can also have oxidation states from +1 to +7 and can form more than one bond by donating valence electrons.

Hydrogen has only one valence electron, but it can form bonds with more than one atom. In the bifluoride ion ([HF2]), for example, it forms a three-center four-electron bond with two fluoride atoms:

[F−H F ↔ F H−F]

Another example is the three-center two-electron bond in diborane (B2H6).

Maximum valences of the elements

Maximum valences for the elements are based on the data from list of oxidation states of the elements. They are shown by the color code at the bottom of the table.

  • v
  • t
  • e

Maximum valences of the elements

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18
Group →
↓ Period
1 1
H
2
He
2 3
Li
4
Be
5
B
6
C
7
N
8
O
9
F
10
Ne
3 11
Na
12
Mg
13
Al
14
Si
15
P
16
S
17
Cl
18
Ar
4 19
K
20
Ca
21
Sc
22
Ti
23
V
24
Cr
25
Mn
26
Fe
27
Co
28
Ni
29
Cu
30
Zn
31
Ga
32
Ge
33
As
34
Se
35
Br
36
Kr
5 37
Rb
38
Sr
39
Y
40
Zr
41
Nb
42
Mo
43
Tc
44
Ru
45
Rh
46
Pd
47
Ag
48
Cd
49
In
50
Sn
51
Sb
52
Te
53
I
54
Xe
6 55
Cs
56
Ba
1 asterisk 71
Lu
72
Hf
73
Ta
74
W
75
Re
76
Os
77
Ir
78
Pt
79
Au
80
Hg
81
Tl
82
Pb
83
Bi
84
Po
85
At
86
Rn
7 87
Fr
88
Ra
1 asterisk 103
Lr
104
Rf
105
Db
106
Sg
107
Bh
108
Hs
109
Mt
110
Ds
111
Rg
112
Cn
113
Nh
114
Fl
115
Mc
116
Lv
117
Ts
118
Og
 
1 asterisk 57
La
58
Ce
59
Pr
60
Nd
61
Pm
62
Sm
63
Eu
64
Gd
65
Tb
66
Dy
67
Ho
68
Er
69
Tm
70
Yb
1 asterisk 89
Ac
90
Th
91
Pa
92
U
93
Np
94
Pu
95
Am
96
Cm
97
Bk
98
Cf
99
Es
100
Fm
101
Md
102
No
Maximum valences are based on the List of oxidation states of the elements


0
1
2
3
4
5
6
7
8
9
Unknown
Background color shows maximum valence of the chemical element

Primordial From decay SyntheticBorder shows natural occurrence of the element

See also

  • Abegg’s rule
  • Oxidation state

References

  1. ^ a b Partington, James Riddick (1921). A text-book of inorganic chemistry for university students (1st ed.). OL 7221486M.
  2. ^ a b IUPAC Gold Book definition: valence
  3. ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
  4. ^ Parkin, Gerard (May 2006). «Valence, Oxidation Number, and Formal Charge: Three Related but Fundamentally Different Concepts». Journal of Chemical Education. 83 (5): 791. doi:10.1021/ed083p791. ISSN 0021-9584.
  5. ^ Harper, Douglas. «valence». Online Etymology Dictionary.
  6. ^ a b Partington, J.R. (1989). A Short History of Chemistry. Dover Publications, Inc. ISBN 0-486-65977-1.
  7. ^ Frankland, E. (1852). «On a New Series of Organic Bodies Containing Metals». Philosophical Transactions of the Royal Society of London. 142: 417–444. doi:10.1098/rstl.1852.0020. S2CID 186210604.
  8. ^ Langmuir, Irving (1919). «The Arrangement of Electrons in Atoms and Molecules». Journal of the American Chemical Society. 41 (6): 868–934. doi:10.1021/ja02227a002.
  9. ^ Magnusson, Eric (1990). «Hypercoordinate molecules of second-row elements: d functions or d orbitals?». J. Am. Chem. Soc. 112 (22): 7940–7951. doi:10.1021/ja00178a014.
  10. ^ Frenking, Gernot; Shaik, Sason, eds. (May 2014). «Chapter 7: Chemical bonding in Transition Metal Compounds». The Chemical Bond: Chemical Bonding Across the Periodic Table. Wiley – VCH. ISBN 978-3-527-33315-8.
  11. ^ Merriam-Webster, Merriam-Webster’s Unabridged Dictionary, Merriam-Webster, archived from the original on 2020-05-25, retrieved 2017-05-11.
  12. ^ «Lesson 7: Ions and Their Names». Clackamas Community College. Archived from the original on 21 January 2019. Retrieved 5 February 2019.
  13. ^ The Free Dictionary: valence
  14. ^ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the «Gold Book») (1997). Online corrected version: (2006–) «Oxidation number». doi:10.1351/goldbook.O04363
  15. ^ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the «Gold Book») (1997). Online corrected version: (2006–) «Lambda». doi:10.1351/goldbook.L03418
  16. ^ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the «Gold Book») (1997). Online corrected version: (2006–) «Oxidation state». doi:10.1351/goldbook.O04365
  17. ^ Frankland, E. (1870). Lecture notes for chemical students(Google eBook) (2d ed.). J. Van Voorst. p. 21.
  18. ^ Frankland, E.; Japp, F.R (1885). Inorganic chemistry (1st ed.). pp. 75–85. OL 6994182M.
  19. ^ Muller, P. (1994). «Glossary of terms used in physical organic chemistry (IUPAC Recommendations 1994)». Pure and Applied Chemistry. 66 (5): 1077–1184. doi:10.1351/pac199466051077. S2CID 195819485.

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