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Question
Answer the following question.
Write one stereochemical difference between SN1 and SN2 reactions.
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Solution
SN1 reactions lead to the formation of racemic mixture whereas SN2 reactions lead to inversion in the configuration of a product.
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RELATED QUESTIONS
Which would undergo SN2 reaction faster in the following pair and why ?

Out of C6H5CH2Cl and C6H5CHClC6H5, which is more easily hydrolysed by aqueous KOH.
In a coordination entity of the type [PtCl2(en)2]2+ which isomer will show optical isomerism?
Arrange the following organic compounds in descending order of their reactivity towards SN1 reaction.
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In the SN1 reaction, racemization takes place. It is due to:
Which of the following statements are correct about the kinetics of this reaction?

(i) The rate of reaction depends on the concentration of only (b).
(ii) The rate of reaction depends on concentration of both (a) and (b).
(iii) Molecularity of reaction is one.
(iv) Molecularity of reaction is two.
Which one is the correct order of nucleophilic strength (pKa) of following nucleophiles?
Optical activity of an enantiomeric mixture is +12.6° and the specific rotation of (+) isomer is +30°. The optical purity is ______ %.
Assertion (A):
undergoes SN2 reactions faster than
.
Reason (R): Iodine is a better leaving group because of its large size.
In the light of the above statements, choose the correct answer from the options given below:
The compound that will undergo SN1 reaction with the fastest rate is:
