• 072920 77839
  • info@smartachievers.in
Menu
Back
  • JEE ADVANCE
  • JEE MAIN
  • NEET
  • BITSAT
  • CBSE BOARD
  • UP BOARD
  • CUET
JEE ADVANCE
  • CLASS XI - XII
  • CRASH COURSE
CRASH COURSE
JEE MAIN
  • CLASS XI - XII
  • CRASH COURSE
CRASH COURSE
NEET
  • CLASS XI - XII
  • CRASH COURSE
BITSAT
  • CLASS XI - XII
CBSE BOARD
  • CLASS IX
  • CLASS X
  • CLASS XI
  • CLASS XII
  • CLASS VI
  • CLASS VII
  • CLASS VIII
UP BOARD
  • CLASS IX
  • CLASS X
  • CLASS XI
  • CLASS XII
CUET
  • CRASH COURSE
Courses


Solution


Q.

In an SN1 reaction on chiral centres, there is              [2015]
1 inversion more than retention leading to partial racemisation  
2 100% retention  
3 100% inversion  
4 100% racemisation  

Ans.

(1)

In case of optically active alkyl halides, SN1 reaction is accompanied by racemisation. The carbocation formed in the slow step being sp2 hybridised is planar and attack of nucleophile may take place from either side resulting in a mixture of products, one having the same configuration and other having inverted configuration.

The isomer corresponding to inversion is present in slight excess because SN1 also depends upon the degree of shielding of the front side of the reacting carbon.