Among the given compounds,choose the two that | vedclass

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(C) Upon ionization,compound $A$ ($3$-bromo$-1-$methylcyclohex$-1-$ene) loses a bromide ion to form the $1-$methylcyclohex$-2-$en$-1-$yl cation.Compou

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$A, B$

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(C) Upon ionization,compound $A$ ($3$-bromo$-1-$methylcyclohex$-1-$ene) loses a bromide ion to form the $1-$methylcyclohex$-2-$en$-1-$yl cation.Compound $B$ ($4$-bromo$-1-$methylcyclohex$-1-$ene) loses a bromide ion to form a secondary carbocation at the $C4$ position.This secondary carbocation undergoes a hydride shift to form the more stable allylic $1-$methylcyclohex$-2-$en$-1-$yl cation,which is the same intermediate as formed from compound $A$.Therefore,compounds $A$ and $B$ yield the same carbocation.

Among the given compounds,choose the two that yield the same carbocation on ionization.

Similar Questions

Assertion : Carbanions like ammonia have pyramidal shape.
Reason : The carbon atom carrying negative charge has an octet of electrons.

Which of the following has an unstable enol form?

In the organic reaction by fission of bond,which intermediate species are formed? Name these species and explain their stability.

The stability of carbanions follows the order:
$I: CH_3CH_2CH_2\bar{C}H_2$
$II: CH_3\bar{C}HCH_2CH_3$
$III: (CH_3)_3\bar{C}$
$IV: CH_3\bar{C}(Ph)CH_2CH_3$

Which one of the carbanions is the least stable?

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