Predict the correct reactivity order of the f | vedclass

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(A) The rate of $S_N1$ reaction is directly proportional to the stability of the carbocation intermediate formed after the departure of the leaving gr

Vedclass · Accepted Answer

$C_6H_5CH_2Br < C_6H_5CH(CH_3)Br < (C_6H_5)_2CHBr < (C_6H_5)_2C(CH_3)Br$

Vedclass · Answer

(A) The rate of $S_N1$ reaction is directly proportional to the stability of the carbocation intermediate formed after the departure of the leaving group $(Br^-)$.$1$. $C_6H_5CH_2^+$: Primary benzylic carbocation (stabilized by one phenyl ring).$2$. $C_6H_5CH(CH_3)^+$: Secondary benzylic carbocation (stabilized by one phenyl ring and one methyl group).$3$. $(C_6H_5)_2CH^+$: Secondary benzylic carbocation (stabilized by two phenyl rings).$4$. $(C_6H_5)_2C(CH_3)^+$: Tertiary benzylic carbocation (stabilized by two phenyl rings and one methyl group).Comparing stability: $C_6H_5CH_2^+ Thus,the reactivity order is $C_6H_5CH_2Br < C_6H_5CH(CH_3)Br < (C_6H_5)_2CHBr < (C_6H_5)_2C(CH_3)Br$.

Predict the correct reactivity order of the following compounds towards $S_N1$ reaction:

Similar Questions

Which of the following alkyl halides gives only one product (excluding stereoisomers) when undergoing an $E_2$ reaction? $(E_2 = \text{elimination bimolecular})$

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Arrange the following organic halides in the correct order of reactivity towards $S_{N}2$ displacement:
$(P) \ (CH_3)_2C(Br)CH_2CH_3$
$(Q) \ BrCH_2(CH_2)_3CH_3$
$(R) \ CH_3CH(Br)(CH_2)_2CH_3$

Identify the major product of the dehydrohalogenation of $CH_3-CH_2-CH(Br)-CH_3$ using an alcoholic base.

In which of the following cases is the yield via $S_{N}2$ mechanism maximum?

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