Chemistry, asked by aliabbas098, 1 month ago

write any four sallent features of SN1 mechanism​

Answers

Answered by technicalmokib
0

Explanation:

An example of a reaction taking place with an S

N

1

reaction mechanism is the hydrolysis of tert-butyl bromide with water forming tert-butanol-

tert-butyl bromide

(CH

3

)

3

C−Br

+2H

2

O⟶

tert-butanol

(CH

3

)

3

C−OH

+Br

+H

3

O

+

The above S

N

1

reaction takes place in three steps-

Formation of a tert-butyl carbocation by separation of a leaving group (Br

) from the carbon atom (this step is slow and reversible)-

(CH

3

)

3

C−Br⟶(CH

3

)

3

C

+

+Br

The carbocation reacts with the nucleophile. The intermediate is an oxonium ion (this reaction step is fast).

(CH

3

)

3

C

+

+H−O−H⟶(CH

3

)

3

C−H−

O

−H

Deprotonation will take place and alcohol will form along with hydronium ion (this reaction step is fast).

(CH

3

)

3

C−H−

O

−H+H−O−H⟶(CH

3

)

3

C−OH+H

3

O

+

Answered by dakshachand19
0

Answer:

An example of a reaction taking place with an SN1 reaction mechanism is the hydrolysis of tert-butyl bromide with water forming tert-butanol-

tert-butyl bromide(CH3)3C−Br+2H2O⟶tert-butanol(CH3)3C−OH+Br−+H3O+

The above SN1 reaction takes place in three steps-

Formation of a tert-butyl carbocation by separation of a leaving group (Br−) from the carbon atom (this step is slow and reversible)-

(CH3)3C−Br⟶(CH3)3C++Br−

The carbocation reacts with the nucleophile. The intermediate is an oxonium ion (this reaction step is fast).

(CH3)3C++H−O−H⟶(CH3)3C−H−O⊕−H

Deprotonation will take place and alcohol will form along with hydronium ion (this reaction step is fast).

(CH3)3C−H−

Explanation:

may its helps you

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