In compound (X),hyperconjugation is present a | vedclass

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(C) Hyperconjugation requires an $\alpha-$hydrogen atom attached to an $sp^2$ hybridized carbon atom. In Toluene $(C_6H_5CH_3)$,the methyl group has t

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Toluene,nitrobenzene

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(C) Hyperconjugation requires an $\alpha-$hydrogen atom attached to an $sp^2$ hybridized carbon atom. In Toluene $(C_6H_5CH_3)$,the methyl group has three $\alpha-$hydrogens attached to the benzene ring,exhibiting hyperconjugation.Resonance effect involves the delocalization of $\pi-$electrons or lone pairs. In nitrobenzene $(C_6H_5NO_2)$,the nitro group is in conjugation with the benzene ring,exhibiting a strong resonance effect ($-M$ effect).Therefore,$X$ is Toluene and $Y$ is nitrobenzene.

In compound $(X)$,hyperconjugation is present and in $(Y)$,resonance effect is present. What are $X$ and $Y$,respectively?

Similar Questions

Which of the following statements is $NOT$ correct?

Which of the following represents the hyperconjugation effect?

Which of the following is not the correct order of inductive effect?

The correct order of stability for the following alkoxides is:
$(A)$ $CH_3CH(NO_2)O^-$
$(B)$ $CH_2=C(NO_2)O^-$
$(C)$ $O_2N-CH=CH-O^-$

For the compound $R-CH=CH_2$,what is the order of the hyperconjugation effect for the group $R$,where $R$ is $CH_3-$,$CH_3CH_2-$,or $(CH_3)_2CH-$?

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