well,a tertiary aolcohol means that it has to be bonded to 3 bonds, which means it cant bond with anything else so no oxygen can bond to it
no reactions will occur
A Tertiary alcohol
benzophenone, or diphenyl ketone, is a ketone. You might have known that when Grignard reagents react with ketones, the product is a tertiary alcohol. CH3CH2MgBr + (C6H5)2CO-----> CH3CH2(C6H5)2COH (a tertiary alcohol) The ammonium chloride solution merely dissolves this alcohol.
Orange ---> Green Primary and secondary alcohols, no reaction with tertiary
Gluconic acid is formed when the aldehyde end of glucose is oxidized.
Water and carbon dioxide.
A Tertiary alcohol
ketone
The product of the oxidation of a primary alcohol is a carboxylic acid.
Because 2- methylcyclohexanol is a secondary alcohol (2 R- groups) and can be oxidized to a ketone quite easity whereas 1- methylcyclohexanol is a tertiary alcohol (3 R- groups) and is not easily oxidized. Tertiary alcohols in general are very difficult to oxidize.
Oxidation of a primary alcohol results in an Aldahyde, 2 molecules of primary alcohol oxidized results in an ether, oxidization of a secondary alcohol end product is a ketone. Oxidation of a primary alcohol results in an Aldahyde, 2 molecules of primary alcohol oxidized results in an ether, oxidization of a secondary alcohol end product is a ketone.
Secondary and tertiary alcohols can form ketones. A primary alcohol will form an aldehyde.
benzophenone, or diphenyl ketone, is a ketone. You might have known that when Grignard reagents react with ketones, the product is a tertiary alcohol. CH3CH2MgBr + (C6H5)2CO-----> CH3CH2(C6H5)2COH (a tertiary alcohol) The ammonium chloride solution merely dissolves this alcohol.
Orange ---> Green Primary and secondary alcohols, no reaction with tertiary
primary alcohol reacts the fastest towards oxidation followed by secondary alcohol and tertiary alcohol.
lacey
Gluconic acid is formed when the aldehyde end of glucose is oxidized.
tertiary