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Question 14 Marks
The molecular orbital theory is based on the principle of a linear combination of atomic orbitals. According to this approach when atomic orbitals of the atoms come closer, they undergo constructive interference as well as destructive interference giving molecular orbitals, i.e., two atomic orbitals overlap to form two molecular orbitals, one of which lies at a lower energy level (bonding molecular orbital). Each molecular orbital can hold one or two electrons in accordance with Pauli's exclusion principle and Hund's rule of maximum multiplicity.
For molecules up to $N _2$, the order of filling of orbitals is:
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Bond order $=\frac{1}{2}$ [bonding electrons - antibonding electrons]
Bond order gives the following information:
I. If bond order is greater than zero, the molecule/ion exists otherwise not.
II. Higher the bond order, higher is the bond dissociation energy.
III. Higher the bond order, greater is the bond stability.
IV. Higher the bond order, shorter is the bond length.

1. Arrange the following negative stabilities of $CN , CN ^{+}$and $CN ^{-}$in increasing order of bond. (1)
2. The molecular orbital theory is preferred over valence bond theory. Why? (1)
3. Ethyne is acidic in nature in comparison to ethene and ethane. Why is it so? (2)
OR
Bonding molecular orbital is lowered by a greater amount of energy than the amount by which antibonding molecular orbital is raised. Is this statement correct? (2)
Answer
1. The increasing order of negative stabilities of $CN , CN ^{+}$and $CN ^{-}$is $CN ^{+}> CN > CN ^{-}$.
2. The molecular orbital theory is preferred over valence bond theory because molecular orbital theory explains the magnetic nature of the molecule.
3. In ethyne, hydrogen atoms are connected to $s p$ hybridized carbon atoms, but in ethene, they are attached to $sp ^2$ hybridized carbon atoms and in ethane, they are attached to $sp ^3$ hybridized carbons.
OR
The given statement is not correct because the bonding molecular orbital is lowered by a lesser amount of energy than the amount by which antibonding molecular orbital is raised.
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Question 24 Marks
The phenomenon of the existence of two or more compounds possessing the same molecular formula but different properties is known as isomerism. Such compounds are called isomers. Compounds having the same molecular formula but different structures (manners in which atoms are linked) are classified as structural isomers. Structural isomers are classified as chain isomer, position isomer, functional group isomer. Meristematic arises due to different alkyl chains on either side of the functional group in the molecule and stereoisomerism and can be classified as geometrical and optical isomerism. Hyperconjugation is a general stabilising interaction. It involves delocalisation of $\sigma$ electrons of the C-H bond of an alkyl group directly attached to an atom of an unsaturated system or to an atom with an unshared p orbital. This type of overlap stabilises the carbocation because electron density from the adjacent $\sigma$ bond helps in dispersing the positive charge.

1. Why Isopentane, pentane and Neopentane are chain isomers?
2. The molecular formula $C _3 H _8 O$ represents which isomer?
3. What type of isomerism is shown by Methoxypropane and ethoxyethane?
OR
Why hyperconjugation is a permanent effect?
Answer
1. Isopentane, pentane and Neopentane are chain isomers because they have a similar molecular formula but a different carbon skeleton.
2. The molecular formula $C _3 H _8 O$ represents positional isomers because they differ in the position of substituent functional group $( OH )$ on the carbon skeleton.
3. Methoxypropane and ethoxyethane are metamers because none of its side are similar to each other.
OR
The $\sigma$ electrons of C-H bond of the alkyl group enter into partial conjugation with the attached unsaturated system or with the unshared p orbital therefore hyperconjugation is permanent effect.
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