24thats the mystery heree
Under specific cond, the substrate X undergoes substitution reaction
and elimination reaction to give products A to D.A and B are
stereoisomers but not enantiomers,C and D are enatiomers.A is not
isomer of C
X +H2O /Heat --------->A + B + C + D
Q1 What should be the structure of X ????
Q2 True/False -: A and B are disteromers and both rotate plane
polarized light.
Q3 True/False -: C and D are elimination products formed by
deprotonation from two different but equivalent α- C of carbocation
intermediate.
Q4 How should be the relative percentage of four products A,B ,C,D
related?
-
UP 0 DOWN 0 0 9
9 Answers
1atleast give formula of A or B or any one thing .da. otherwise how can we do ?
1no something is seriously wrong wid this question.....
did U make the question ??? [3]
24i didnt make this question...........I found it in my brother's copy......
1X is three degree halide
false
false
A>B>C=D
here i am taking as A the trans isomer and one assumption i have taken is X is mono chloro derivative of an alkane
24I am posting the answers.......plzzz give me solutions........
1) 3 degree halide
2) True
3) True
4) A≠B but C=d