SN 1 reaction is faster inA- CH 3 CH 2 ClB- CH 3 CH 3- CH - ClCH 3C - CH 3- C - ClCH 3D- CH 3- CH - Cl

The correct option is C SN^1 meachanism proceeds through carbocation intermediate. CH_3 CH_3|CH_3|C Cl Provides stable carbocation intermediate because it has ...

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Byju's Answer

Standard XII

Chemistry

Cyclic Hydrocarbons

SN 1 reaction...

Question

$S N^{1}$ reaction is faster in

$C H_{3} C H_{2} C l$

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Solution

The correct option is C

$S N^{1}$ meachanism proceeds through carbocation intermediate.

$C H_{3} - C H_{3} | C | C H_{3} - C l$ Provides stable carbocation intermediate because it has tertiary carbon.

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Similar questions

$S_{N}^{1}$ reaction is fastest in

Q. Out of

\begin{matrix} C H_{3} - & C H & - C H_{2} - C l | C H_{3} \end{matrix}

and

\begin{matrix} C H_{3} - C H_{2} - & C H & - C l | C H_{3} \end{matrix}

which is more reactive towards

S_{N} 1

reaction and why?

Q. Which of the following reaction is example of

S_{N} 2

reaction using

c o n c . H C l :

(a) C H_{3} - C H_{2} - O H A n h y Z n C l_{2} / △ - -------- \to C H_{3} - C H_{2} - C l

(b) C H_{3} - C H_{3} | C | C H_{3} - C H_{2} O H A n h y Z n C l_{2} / △ - -------- \to C H_{3} - C H_{1} | C | C H_{3} - C H_{2} - C H_{3}

(c) C H_{3} - O H | C | C H_{3} - C H_{3} A n h y Z n C l_{2} / △ - -------- \to C H_{3} - C l | C | C H_{3} - C H_{3}

(d) C H_{2} = C H - C H_{2} - O H A n h y Z n C l_{2} / △ - -------- \to C H_{2} = C H - C H_{2} - C l

Q. Among the given reaction which is faster & why?

(i)

M e - C | C l H - M e a l c . K O H - ---- \to C H_{3} - C H = C H_{2}

(ii)

C H_{3} - C H_{2} - C H_{2} - C l a l c . K O H - ---- \to C H_{3} - C H = C H_{2}

Q. Select the member of each pair that shows faster rate of

S_{N} 2

reaction with

K I

in acetone.

(a)

C H_{3} - C H_{2} - C H_{2} - C H_{2} - C l a n d C H_{3} - C H ∣ C H_{3} - C H_{2} - C l

(I) (I I)

(b)

C H_{3} - C H_{2} - C H_{2} - C l a n d C H_{3} - C H_{2} - C H_{2} - B r

(I) (I I)

(c)

C H_{3} - C H ∣ C H_{3} - C H_{2} - C H_{2} - C l a n d C H_{3} - C H_{3} ∣ C ∣ C H_{3} - C H_{2} C l

(I) (I I)

(d)

C H_{3} - C H_{2} - C H_{2} - B r ∣ C H - C H_{3} a n d C H_{3} - C H_{3} ∣ C H - C H_{2} - B r ∣ C H - C H_{3}

(I) (I I)

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SN1 reaction is faster in

The correct option is C SN1 meachanism proceeds through carbocation intermediate. CH3−CH3|C|CH3−Cl Provides stable carbocation intermediate because it has tertiary carbon.

$S N^{1}$ reaction is faster in

The correct option is C

$S N^{1}$ meachanism proceeds through carbocation intermediate.

$C H_{3} - C H_{3} | C | C H_{3} - C l$ Provides stable carbocation intermediate because it has tertiary carbon.