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 :
[b] The tertiary alkyl halide undergoes elimination reaction to give alkenes. \[C{{H}_{3}}-\underset{C{{H}_{3}}}{\overset{C{{H}_{3}}}{\mathop{\underset{|}{\overset{|}{\mathop{C}}}\,}}}\,-X+NaO{{C}_{2}}{{H}_{5}}\xrightarrow{{}}\underset{2-methyl\,\,propene}{\mathop{C{{H}_{3}}-\overset{C{{H}_{3}}}{\mathop{\overset{|}{\mathop{C}}\,}}\,=C{{H}_{2}}}}\,\]
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