In Williamson synthesis of mixed ether having a primary and a tertiary alkyl group,if a tertiary halide is used,then:
- ARate of reaction will be slow due to slow cleavage of carbon-halogen bond.
- BAlkene will be the main product.
- CSimple ether will form instead of mixed ether.
- DExpected mixed ether will be formed.
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Similar Questions
Which of the following compounds has no reaction with sodium metal?
Give the major products that are formed by heating each of the following ethers with $HI$.
$(i)$ $CH_3-CH_2-CH(CH_3)-CH_2-O-CH_2-CH_3$
$(ii)$ $CH_3-CH_2-CH_2-O-C(CH_3)_2-CH_2-CH_3$
$(iii)$ $C_6H_5-CH_2-O-C_6H_5$
$(i)$ $CH_3-CH_2-CH(CH_3)-CH_2-O-CH_2-CH_3$
$(ii)$ $CH_3-CH_2-CH_2-O-C(CH_3)_2-CH_2-CH_3$
$(iii)$ $C_6H_5-CH_2-O-C_6H_5$
Difficult
View SolutionEthyl chloride reacts with sodium ethoxide to form a compound $A$. Which of the following reactions also yields $A$?
Consider the reaction sequence:
Dimethyl ketone $\xrightarrow[(ii) H_2O]{(i) CH_3MgCl} X$ $\xrightarrow[(ii) CH_3Br]{(i) Na} Y$
How many $sp^3$ carbons are present in $Y$?
Dimethyl ketone $\xrightarrow[(ii) H_2O]{(i) CH_3MgCl} X$ $\xrightarrow[(ii) CH_3Br]{(i) Na} Y$
How many $sp^3$ carbons are present in $Y$?
Which products are obtained when methoxy ethane is heated with $HI$?
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