Question

How many isomers can be obtained by free radical chlorination of $2,2,4-trimethylpentane$ ?

Answer 1

Hint : We know that the phenomenon of existence with the same molecule formula of two or more compounds but exhibit different physical and chemical properties is known as isomers and the compound which shows isomerism phenomenon is an isomer.

Complete Step By Step Answer:
Monochlorination of alkanes means the substitution of one chlorine atom by replacing one hydrogen atom. This reaction is a radical substitution reaction in alkanes. The number of monochloro isomers depends on the types of hydrogen atoms present in $2,2,4-trimethylpentane.$ Based on the organic compounds and its functional groups; this isomerism is mainly classified into structural and stereoisomerism. Chlorination of alkane undergoes in the presence of UV-light.
The free radical chlorination of $2,2,4-2,2,4-~trimethylpentane$ gives a total $6$ isomers. Four types of radicals possible out of which two chlorination products have chiral carbon so both R and S form possible. In all of the above products chlorine is added at free radical carbon.
In $2,2,4-trimethylpentane.$ different types of hydrogen atoms will present like, there are four types of hydrogen atoms as one type of two primary hydrogen atoms, one type of secondary hydrogen atom, and one type of tertiary hydrogen atom. Because of the four different hydrogen atoms of 2-methyl butane, there is a possibility of replacement of hydrogen atom with chlorine atom during monochlorination six structural isomers will form as monochloro products.

Note :
There are three types of structural isomers observed in alkanes. They are functional group isomers, chain isomers, functional group isomers, and positional isomers. When monochlorination occurs in alkanes, the possibility of constitutional isomers depends on the structural formula and the orientation of hydrogen molecules attached to carbon atoms.