(C) The $S_N1$ mechanism proceeds through the formation of a planar carbocation intermediate. Because the carbocation is planar,the nucleophile can at

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(C) The $S_N1$ mechanism proceeds through the formation of a planar carbocation intermediate. Because the carbocation is planar,the nucleophile can attack from either the front side or the back side with equal probability. This leads to the formation of both enantiomers in equal amounts,resulting in a racemic mixture.

Class 12 Chemistry Haloalkanes and Haloarenes Properties of Haloalkanes

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What is the primary product of an $S_N1$ reaction on an optically active substance?

A
Retention of configuration
B
Inversion of configuration
C
Racemic mixture
D
No product

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Class 12 Questions

Class 12

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Chapter

Haloalkanes and Haloarenes

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Properties of Haloalkanes

$CH_3-C(CH_3)=CH-CH_2-CH_2-Cl \xrightarrow[CaCO_3]{H_2O} (X)$
The major product $(X)$ of the above reaction is:

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The product $(B)$ of the reaction is:

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When $32.25 \ g$ of ethyl chloride is dehydrohalogenated,it gives $50\%$ yield of alkene. What is the mass of the product in $g$? (Atomic mass of $Cl = 35.5$)

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Which of the following represents the Wurtz-Fittig reaction?

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The product formed when toluene is heated in light with $Cl_2$ and in the absence of a halogen carrier is:

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What is the primary product of an $S_N1$ reaction on an optically active substance?

Similar Questions

$CH_3-C(CH_3)=CH-CH_2-CH_2-Cl \xrightarrow[CaCO_3]{H_2O} (X)$The major product $(X)$ of the above reaction is:

The product $(B)$ of the reaction is:

When $32.25 \ g$ of ethyl chloride is dehydrohalogenated,it gives $50\%$ yield of alkene. What is the mass of the product in $g$? (Atomic mass of $Cl = 35.5$)

Which of the following represents the Wurtz-Fittig reaction?

The product formed when toluene is heated in light with $Cl_2$ and in the absence of a halogen carrier is:

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$CH_3-C(CH_3)=CH-CH_2-CH_2-Cl \xrightarrow[CaCO_3]{H_2O} (X)$
The major product $(X)$ of the above reaction is: