From the following,identify the groups that e | vedclass

Name: Exam Paper Generator | JEE NEET Paper Generator | Vedclass
Brand: Vedclass
Rating: 5 (35 reviews)

Question

(C) Groups that exhibit the negative resonance $(-R)$ effect are those that withdraw electron density from the conjugated system. These groups typical

Vedclass · Accepted Answer

$A, D, E$ only

Vedclass · Answer

(C) Groups that exhibit the negative resonance $(-R)$ effect are those that withdraw electron density from the conjugated system. These groups typically contain multiple bonds with electronegative atoms.$(A)$ Formyl $(-CHO)$: $-C(=O)H$ ($-R$ effect)$(B)$ Amino $(-NH_2)$: $+R$ effect due to lone pair on $N$.$(C)$ Alkoxy $(-OR)$: $+R$ effect due to lone pair on $O$.$(D)$ Cyano $(-CN)$: $-C \equiv N$ ($-R$ effect)$(E)$ Nitro $(-NO_2)$: $-NO_2$ ($-R$ effect)Therefore,$A, D,$ and $E$ exhibit the $-R$ effect.

From the following,identify the groups that exhibit negative resonance $(-R)$ effect when attached to a conjugated system: $(A)$ formyl,$(B)$ amino,$(C)$ alkoxy,$(D)$ cyano,$(E)$ nitro

Similar Questions

Steric inhibition of resonance takes place in

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

Represent the three types of electron movement in organic reactions.

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

Rank the following compounds in order of increasing acidity (weakest acid first).

Vedclass Test Series

Exam Paper Generator

Online Exam Module