carbonyl group

With its free carbonyl group, it is a reducing sugar.

The position of the carbonyl group is usually denoted by a number.

It was found that the carbonyl group is the active centre towards reduction.

Structure of the carbonyl group using a molecular orbital approach.

The carbonyl group then locks the ring permanently in place.

It will always react with carbonyl groups, and this cannot be discouraged by any means.

Carbonyl groups have lower anharmonicities. Their value is about 10 cm−1, for both free and associated species.

In many nucleophilic reactions, addition to the carbonyl group is very important.

This stability would be lost by addition of a reagent to the carbonyl group.

These compounds are formed by formal addition of an alcohol to the carbonyl group.

Meerwein–Pondorff reduction of product carbonyl groups was also observed.

The following figure shows a ligated metal attached to a carbonyl group.

One study shows that the success depends critically on the accessibility of the carbonyl group.

This makes the carbonyl group more susceptible to attack by the peroxyacid.

It functions as an antiknock agent by the action of the carbonyl groups.

This species reacts with the carbonyl group in a nucleophilic addition.

It uses a catalyst to add a carbonyl group to methanol.

Alkanals have the carbonyl group at the end of the saturated carbon chain.

Aldehydes carry a hydrogen atom next to their carbonyl group.

Reacting a carbonyl group with 1,2-ethanedithiol converts it to a 1,3-dithiolane, as detailed below.

Its reactions with nucleophiles often involves the reaction of both carbonyl groups.

The first pathway has the peroxyacid attack the oxygen of the carbonyl group.

The sulfur atom is within the ring system and adjacent to a carbonyl group.

The carbonyl group in 1 takes a proton from hydrochloric acid.

Photocycloaddition of isobutylene to the carbonyl group was observed with 1 and 2.