In which of the following molecules do all th | vedclass

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(C) To exhibit all three effects (inductive,mesomeric,and hyperconjugation),a molecule must have a conjugated system (for mesomeric effect),an electro

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$1-$acetyl$-2-$methylcyclohex$-1-$ene

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(C) To exhibit all three effects (inductive,mesomeric,and hyperconjugation),a molecule must have a conjugated system (for mesomeric effect),an electronegativity difference (for inductive effect),and $\alpha$-hydrogen atoms attached to an $sp^3$ hybridized carbon adjacent to a $\pi$-system (for hyperconjugation).$1$. In $1$-acetyl-$2$-methylcyclohex-$1$-ene,the methyl group attached to the double bond provides hyperconjugation due to $\alpha$-$H$ atoms.$2$. The carbonyl group $(-COCH_3)$ is conjugated with the double bond,exhibiting the mesomeric effect $(-M)$.$3$. The electronegativity difference between the carbons of the double bond and the attached substituents creates an inductive effect ($-I$ or $+I$).Thus,this molecule satisfies all three conditions.

In which of the following molecules do all the effects,namely inductive,mesomeric,and hyperconjugation,operate?

Similar Questions

Which of the following represents the hyperconjugation effect?

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

Which one of the following represents the hyperconjugation effect?

Which of the following is not correct?

In which of the following organic compounds are all effects (i.e.,mesomeric effect,hyperconjugation effect,and inductive effect) present?

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