A) Rate of reaction will be slow due to slow cleavage of carbon ? halogen bond
B) Alkene will be the main product
C) Simple ether will form instead of mixed ether
D) Expected mixed ether will be formed
Correct Answer: B
Solution :
The tertiary alkyi halide undergo elimination reaction to give alkenes \[C{{H}_{3}}-\underset{C{{H}_{3}}}{\overset{C{{H}_{3}}}{\mathop{\underset{|}{\overset{|}{\mathop{C}}}\,}}}\,-X+NaO{{C}_{2}}{{H}_{5}}\xrightarrow{{}}\] \[\underset{2-\text{methyl}\,\,\text{propence}}{\mathop{C{{H}_{3}}-\overset{C{{H}_{3}}}{\mathop{\overset{|}{\mathop{C}}\,}}\,=C{{H}_{2}}}}\,\]
You need to login to perform this action.
You will be redirected in
3 sec
