The reaction of diethyl ether with one equivalent of HI at room temperature primarily yields:

Williamson’s synthesis is used for the preparation of

What is the hybridisation of carbon and oxygen in electronic structure of ether?

Which of the following is simple ether?

Arrange the following ethers in decreasing order of their reactivity towards cleavage with HI:

(i) $CH_3OCH_3$

(ii) $CH_3OCH_2CH_3$

(iii) $(CH_3)_2CHOCH(CH_3)_2$

(iv) $CH_3OC(CH_3)_3$

Williamson’s synthesis is used to prepare

Ethers are not distilled to dryness for fear of explosion. This is due to formation of:

Ethers are quite stable towards:

Anisole can be prepared by the action of methyl iodide on sodium phenate. The reaction is called

One mole of an organic compound $A$ with the formula ${{\rm{C}}_3}{{\rm{H}}_8}{\rm{O}}$ reacts completely with two moles of HI to form $X$ and $Y$. When $Y$ is boiled with aqueous alkali it forms $Z$. $Z$ answers the iodoform test. The compound $A$ is

The boiling points of thio-ethers are…than those of ether.