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Hydrogen octet rule exceptions

Arrange the remaining electrons as lone pairs or create double or triple bonds to satisfy the octet rule. Exceptions Hydrogen satisfies the duet (two) rule, and boron and aluminum satisfy the six-electron rule. [Pg.79]

In most of their covalent compounds, the representative elements follow the octet rule, except that hydrogen always shares only two electrons. [Pg.287]

These examples illustrate the principle that atoms in covalently bonded species tend to have noble-gas electronic structures. This generalization is often referred to as the octet rule. Nonmetals, except for hydrogen, achieve a noble-gas structure by sharing in an octet of electrons (eight). Hydrogen atoms, in molecules or polyatomic ions, are surrounded by a duet of electrons (two). [Pg.168]

In the N — A = S rule, only the valence electrons are counted. This rule assumes that all atoms, except hydrogen, are going to obey the octet rule. [Pg.135]

In a compound that is an exception to the octet rule, there is usually only one atom, other than hydrogen, that is an exception. There are few nonhydrogen compounds with more than one exception present. [Pg.140]

As mentioned previously, in 1916, Lewis noted that noble gases were particularly stable and did not form compounds. Lewis used these facts to formulate the octet rule. The noble gases have their outer electron shell filled with eight electrons. (Helium is an exception with only two electrons in its outer shell.) The octet rule says that the most stable electron configuration of an atom occurs when that atom acquires the valence electron configuration of a noble gas. That is, when an atom can acquire eight (octet) electrons in its valence shell (or two for hydrogen to become like helium). [Pg.75]

Nonbonded electrons are / v / usually not shown in condensed structures. Atoms in organic molecules (except hydrogen) generally obey the octet rule, so any atom with fewer than four bonds must have a number of non-bonded electron pairs equal to four minus the number of bonds. For example, the oxygen in an alcohol has 4 — 2 = 2 nonbonded electron pairs. [Pg.1007]

Make octets around all surrounding atoms (not the central atom). Use the octet rule to fill in all 8 dots on all atoms surrounding the central atom (the one exception being hydrogen, which should only have two). [Pg.118]

Most of the common elements in organic compounds—C, N, O, and the halogens— follow the octet rule. Hydrogen is a notable exception, because it accommodates only two electrons in bonding. Additional exceptions include boron and beryllium (second-row elements in groups 3A and 2A, respectively), and elements in the third row (particularly phosphorus and sulfur). [Pg.19]

The electron demand is two for each hydrogen and eight for all other atoms usually considered in organic chemistry. (The tendency of most atoms to acquire eight valence electrons Is known as the octet rule.) For elements in group IMA (e.g., B, AI, Ga), the electron demand is six. Other exceptions are noted, as they arise, in examples and problems. [Pg.2]

Octet rule—The octet rule states that all atoms, with the exception of hydrogen, strive to acquire eight electrons in their valence shell. [Pg.112]

Distribute the electron dots so that each atom, except for hydrogen, beryllium, and boron, satisfies the octet rule. [Pg.219]

Count the number of electrons surrounding each atom. Except for hydrogen, beryllium, and boron, all atoms must satisfy the octet rule. Check that the number of valence electrons is still the same number you determined in step 1. [Pg.219]

For both molecules, be sure that all atoms, except hydrogen, obey the octet rule. [Pg.229]

Hydrogen cannot form an octet it requires only two electrons to achieve the configuration of the noble gas, helium. Except for helium, all the noble gases have an octet of electrons in their valence shells, and this is why the phrases noble gas configuration and octet of electrons are often used interchangeably. The octet rule isn t perfect, but it is a useful guide. [Pg.261]

The i-block elements (with the exceptions of H and He) do not have sufficient electrons for hypervalent bonding. Transition metals can use d orbitals in their bonding, and thus do not follow the octet rule. Therefore, with the exception of hydrogen bonding, the central atom in a hypervalent system must be a / -block element. Within the p block, two obvious issues are how the bond strengths change as the central atom A is varied across or down the periodic table. Sufficient data is currently available to begin to define these periodic trends. [Pg.73]

The product of the first step is not a carbocation rather, it is a cyclic bromonium ion because bromine s electron cloud is close enough to the other sp carbon to engage in bond formation. The cyclic bromonium ion is more stable than the carbocation would have been, since all the atoms (except hydrogen) in the bromonium ion have complete octets, whereas the positively charged carbon of the carbocation does not have a complete octet. (To review the octet rule, see Section 1.3.)... [Pg.158]

Explain the octet rule. Why are hydrogen and helium exceptions to the octet rule ... [Pg.199]

Ans. Step 1. Consider the probable arrangement of atoms. In this situation, there are three different types of atoms. However, we note that hydrogen, an exception to the octet rule, is terminal in a Lewis formula, and that carbon is unique among the remaining atoms. A good first guess is that carbon is the central atom to which all others are bonded ... [Pg.74]

However, the octet rule is only a heuristic or rule of thumb. There are plenty of exceptions, including compounds such as carbon monoxide (CO) and borane (BHj). Transition metals commonly form a range of ions (iron, for example, commonly exists in compounds as both Fe + and Fe +). A key point is that because most substances stable enough to be found in our normal surroundings, or indeed in chemistry laboratories, have electronic structures that already obey the octet rule (as in the hydrogen and fluorine example shown in Figure 3.4), it is of no help in explaining why they do or do not react. [Pg.99]

Under the headline restricted chemistry (RC) we collect all compounds whose atoms do not carry any charge or unpaired electron, and obey (except hydrogen) the octet rule,... [Pg.27]

Numerous molecules contain only boron and hydrogen, a family of compounds called boranes. The simplest borane is BHg. This molecule contains only six valence electrons and is tiierefore an exception to tile octet rule. - (Section 8.7) As a result, BHg reacts witii itself to form dtboraiie (B2H6). This reaction can be viewed as a Lewis acid-base reaction (Section 16.11), in which one B—H bonding pair of electrons in each BHg molecule is donated to the other. As a result, diborane is an unusual molecule in which hydrogen atoms appear to form two bonds (Figure 22.55 ). [Pg.909]

The octet rule generally apphes to all main-group elements except hydrogen and hthium. Each of these elements achieves stability when it has two electrons (a duet) in its outermost shell. [Pg.326]

Atoms with eight valence electrons are particularly stable and are said to have an octet. Atoms such as hydrogen, helium, lithium, and beryllium are exceptions to the octet rule as they achieve stability when their outermost shell contains two electrons—a duet. A chemical bond is the sharing or transfer of electrons to attain stable electron configurations among the bonding atoms. [Pg.764]

There are a number of general exceptions to the octet rule electron deficient compounds in which the central atom has an incomplete octet, free radicals (with an unpaired electron), molecules whose central atom is surrounded by more than eight electrons (an expanded octet) and compounds of hydrogen and the transition metals (d-block) and lanthanoids (f-block). [Pg.117]


See other pages where Hydrogen octet rule exceptions is mentioned: [Pg.59]    [Pg.82]    [Pg.224]    [Pg.251]    [Pg.26]    [Pg.25]    [Pg.156]    [Pg.111]    [Pg.85]    [Pg.4]    [Pg.224]    [Pg.953]    [Pg.336]    [Pg.987]    [Pg.259]    [Pg.104]    [Pg.68]    [Pg.134]    [Pg.173]   
See also in sourсe #XX -- [ Pg.19 ]

See also in sourсe #XX -- [ Pg.17 ]




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