मराठी

Sn1 Reactions Are Accompanied by Racemization in Optically Active Alkyl Halides.

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प्रश्न

SN1 reactions are accompanied by racemization in optically active alkyl halides.

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उत्तर

In SN1 reaction, formation of carbocation as an intermediate takes place. This carbocation has sp2-hybridised and planar structure. This planar carbocation is attacked by nucleophile from both the sides equally to form d and l isomers in equal proportion. Such products are called racemic mixture. Hence, SN1 reactions are accompanied by racemisation in optically active alkyl halides.

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2015-2016 (March) Delhi Set 3

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संबंधित प्रश्‍न

Write the structure of an isomer of compound C4H9Br which is most reactive towards SN1 reaction


Which would undergo SN2 reaction faster in the following pair and why ?


Arrange the compounds of the following set in order of reactivity towards SN2 displacement:

1-Bromo-3-methylbutane, 2-Bromo-2-methylbutane, 2-Bromo-3-methylbutane


What happens when ethyl chloride is treated with aqueous KOH?


The stability order for carbocation is _______.

(A) 2° > 3° > 1° 

(B) 3° > 2° > 1°

(C) 3° > 1° > 2°

(D) 1° > 3° > 2°


Which one of the following halogen compounds is difficult to be hydrolysed by SN1 mechanism?


Elimination reactions (especially β-elimination) are as common as the nucleophilic substitution reaction in case of alkyl halides. Specify the reagents used in both cases.


Match the reactions given in Column I with the types of reactions given in Column II.

  Column I Column II
(i) (a) Nucleophilic aromatic substitution
(ii) \[\begin{array}{cc}
\ce{CH3 - CH = CH2 + HBr -> CH3 - CH - CH3}\\
\phantom{............................}|\phantom{}\\
\phantom{.............................}\ce{Br}\phantom{}
\end{array}\]
(b) Electrophilic aromatic substitution
(iii) (c) Saytzeff elimination
(iv) (d) Electrophilic addition
(v) \[\begin{array}{cc}
\ce{CH3  CH2 CH CH3 ->[alc.KOH] CH3  CH = CH CH3}\\
\phantom{}|\phantom{..........................}\\
\phantom{}\ce{Br}\phantom{........................}
\end{array}\]
(e) Nucleophilic substitution (SN1)

The major product formed in the following reaction is:


Inversion of configuration occurs in ______.


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