Mild oxidation of a secondary alcohol will produce a ketone; strong oxidation, such as burning, can produce carbon dioxide and water.
The product of a secondary alcohol oxidation is a ketone.
C.a ketone.
This group is C=O.
a ketone
aldehydes
All primary (10) alcohols may be oxidized to aldehydes.
Orange ---> Green Primary and secondary alcohols, no reaction with tertiary
Camphor is a ketone.It is the oxidation product of borneol, which is a secondary alcohol. Primary alcohols when they are oxidized can either produce carboxylic acids or aldehydes. However, since borneol is secondary, it cannot be oxidized to produce an aldehyde or carboxylic acid.Secondary alcohols, on the other hand, will produce ketones. Since borneol is a secondary alcohol, it cannot be oxidized to make an aldehyde which means that camphor must be a ketone.Here is a link to the reaction that I'm talking about:http://img41.imageshack.us/i/primaryohoxidat2.png/Hope that answers your question.
Borane takes aldehydes to primary alcohols and ketones to secondary alcohols it also reduces esters but only slowly
It is used to distinguish between primary,secondary & tertiary alcohols
Orange ---> Green Primary and secondary alcohols, no reaction with tertiary
All primary (10) alcohols may be oxidized to aldehydes.
Secondary and tertiary alcohols can form ketones. A primary alcohol will form an aldehyde.
Camphor is a ketone.It is the oxidation product of borneol, which is a secondary alcohol. Primary alcohols when they are oxidized can either produce carboxylic acids or aldehydes. However, since borneol is secondary, it cannot be oxidized to produce an aldehyde or carboxylic acid.Secondary alcohols, on the other hand, will produce ketones. Since borneol is a secondary alcohol, it cannot be oxidized to make an aldehyde which means that camphor must be a ketone.Here is a link to the reaction that I'm talking about:http://img41.imageshack.us/i/primaryohoxidat2.png/Hope that answers your question.
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.
ketone
Borane takes aldehydes to primary alcohols and ketones to secondary alcohols it also reduces esters but only slowly
It is used to distinguish between primary,secondary & tertiary alcohols
Yes. Any compound containing an R-OH group will have a name ending in "ol". These are all alcohols.
You can only make any ketone from any secondary alcohol by using PCC, Jones reagent, or NaCr2O4 in acid as a reagent.
secondaryPentan-3-olsecondaryPentan-2-olsecondary3-Methylbutan-2-ol
primary alcohol reacts the fastest towards oxidation followed by secondary alcohol and tertiary alcohol.