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what is the best name for the following compound

6-For the reaction the alcohol product is classified as a CH --Primary Alcohol b-Secondary Alcohol e-Tertiary Alcohol d-Quate
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Answer #1

#6: The alcohol (-OH) group is attached to a C atom to which 2 alkyl groups and 1H atom is attached. Due to the attachment of 2 alkyl groups and 1H, it is a secondary alcohol.

#7: According to Zaitsev's rule, the carbocation intermediate forms the double bond towards the most substituted carbon atom. Because a double bonded alkene formed towards the most substituted C atom is more stable.

Hence option (a) is correct.

#8: During the conversion of 2-bromopropane to propan-2-ol, the -Br group of 2-bromopropane is substituted by an -OH group.

-Br being a leaving group, leaves the carbon chain to form a carbocation intermediate. The -OH (as H2O) acts as nucleophile and attacks the carbocation intermediate to form the desired product.

Hence this is a (d): Nucleophilic substitution reaction.

#9: Removal of H is called oxidation, where as addition of H is called reduction. Also addition of O is called oxidation and removal of O is called reduction.

When an alcohol is converted to an aldehyde or ketone, H is removed. Hence (a) and (b) are oxidation.

When aldehyde converts to acid, O is being added. Hence (c) is also oxidation.

In (d), H is added to propene to reduce it to propane. Hence (d) is a reduction reaction.

#10: (a) and (b) are oxidation reaction.

(d) is a nucleophilic substitution reaction, in which -OH group is substituted by a -Br group.

In (c), H2O is eliminated from propan-1-ol to form propene, an alkene.

Hence (c) is the correct option.

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