The organic chloro compound, which shows complete
stereochemical inversion during a SN2 reaction, is
(a) (C₂H₅)₂CHCl (b) (CH₃)₃CCl
(c) (CH₃)₂ CHCl (d) CH₃Cl
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The organic chloro compound, which shows complete
stereochemical inversion during a SN2 reaction, is
(a) (C₂H₅)₂CHCl
(b) (CH₃)₃CCl
(c) (CH₃)₂ CHCl
(d) CH₃Cl
Answered by
0
CH₃Cl is the correct option.
Explanation:
- SN2 or the nucleophilic substitution bimolecular is the reaction.
- In this reaction, the substitution that occurs is nucleophilic substitution and it involves both the leaving group and attacking group at the same time.
- The intermediate that is formed in case of a nucleophilic substitution is of carbonation nature, and secondary and tertiary carbons are much more stable than 0° or primary carbon atoms because of the +I effect.
- So, the carbon with least hindrance and least +I effect will undergo SN2 most easily.
- So. Here, among the options given, the methyl chloride undergoes the nucleophilic substitution most easily.
For more information about nucleophilic substitution,
https://brainly.in/question/4550474
Ch3f ch3cl ch3br ch3i increasing reactivity towards nucleophilic substitution and increasing order of dipole moment
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