What are $X$ and $Y$ in the following reaction?
$(CH_3)_3COCH_3 + HI \rightarrow X + Y$

Give the common and $\rm {IUPAC}$ names for the following ether compounds:
$(i) \ CH_3OCH_3$
$(ii) \ C_2H_5OC_2H_5$
$(iii) \ C_6H_5OC_6H_5$
$(iv) \ CH_3OCH_2CH_2CH_3$
$(v) \ CH_3OCH(CH_3)_2$
$(vi) \ C_6H_5OCH_3$
$(vii) \ C_6H_5OCH_2CH_3$
$(viii) \ C_6H_5O(CH_2)_6CH_3$
$(ix) \ C_6H_5OCH_2CH_2CH(CH_3)_2$
$(x) \ CH_3OCH_2CH_2OCH_3$
$(xi) \ C_2H_5OCH_2CH_2OC_2H_5$
$(xii) \ CH_3OCH_2CH_2CH_2OCH_3$
$(xiii) \ CH_3OCH_2CH_2OC_2H_5$
$(xiv) \ \text{Cyclohexyl methyl ether}$

An ether $(A)$,$C_5H_{12}O$,when heated with excess of hot concentrated $HI$ produced two alkyl halides which when treated with $NaOH$ yielded compounds $(B)$ and $(C)$. Oxidation of $(B)$ and $(C)$ gave a propanone and an ethanoic acid respectively. The $IUPAC$ name of the ether $(A)$ is

Illustrate with examples the limitations of Williamson synthesis for the preparation of certain types of ethers.

Which reagent is used for the electrophilic aromatic bromination of methyl phenyl ether (anisole)?

Write the mechanism of the reaction of $HI$ with methoxymethane.