`(CH_(3))_(3)C-O-CH_(3)+HIto(CH_(3))_(3)Cl+CH_(3)OH` Justify the preferential formation of the products.

Give reason : (CH_(3))_(3)C-O-CH_(3) on reaction with HI gives (CH_(3))_(3)C-I and CH_(3)-OH as the main products and not (CH_(3))_(3)C-OH and CH_(3)-I

The following is not an appropeiate reaction for the preparation of tert - butyl methyl ether : CH_(3)ONa+(CH_(3))_(3)C-Cl to(CH_(3))_(3)C-OCH_(3) Write a suitable reaction for the preparation of tert - butyl methyl ether, specifying the names of reagents used Justify your answer in both cases.

The following is not an appropeiate reaction for the preparation of tert - butyl methyl ether : CH_(3)ONa+(CH_(3))_(3)C-Cl to(CH_(3))_(3)C-OCH_(3) What would be the major product of the given reaction ?

CH_3CH_2CH_2OH is the functional isomer of:

CH_(3)CHClCH_(2)CH_(3) or CH_(3)CH_(2)CH_(2)Cl Which one undergoes SN_(2) substitution reaction faster and why?

A solution of KOH hydrolyses CH_(3)CHClCH_(2)CH_(3) and CH_(3)CH_(2)CH_(2)CH_(2)Cl . Which one of these is more easily hydrolysed?

IUPAC name of (CH_3)_3C-CH=CH_2 is:

Consider the following reaction, (CH_(3))_(3)CBrunderset(-H_(2)O,-KBr)overset("Alc. KOH")rarr(CH_(3))_(2)C=CH_(2) This is an example of