Etherates are:

Methyl vinyl ether,$H_2C=CH-OCH_3$,reacts with $Br_2/CH_3OH$. If methanol is reacting as water would,and if this reaction follows a typical mechanism of electrophilic addition,what would be the expected product?

Complete the following reaction sequence.
$CH_3-CO-CH_3$ $\xrightarrow[(ii) H_2O]{(i) CH_3MgBr} [A]$ $\xrightarrow{Na, \text{Ether}} [B]$ $\xrightarrow{CH_3-Br} [C]$

Explain the fact that in aryl alkyl ethers $(i)$ the alkoxy group activates the benzene ring towards electrophilic substitution and $(ii)$ it directs the incoming substituents to ortho and para positions in the benzene ring.

What is obtained when sodium ethoxide and ethyl iodide are heated together?

Which of the following ethers, on hydrolysis, gives two different products that are successive members of the homologous series?