Synthesis of Aldehydes - Oxidation of Primary Alcohols:

Synthesis of Aldehydes and Ketones
Zero degree and primary alcohols are oxidized with pyridinium chlorochromate to form aldehydes. Secondary alcohols are oxidized with sodium dichromate, potassium dichromate, potassium permanganate, sodium hypochlorite, nitric acid, chromium trioxide, or pyridinium chlorochromate to ketones. Benzene reacts with aluminum chloride and an acid halide to form a ketone. Alkenes are oxidized to aldehydes and / or ketones with ozone. Acid chlorides are reduced to aldehydes with lithium aluminum tri(t-butoxy) hydride. Acid chlorides react with dialkyl lithium cuprates to yield ketones.

Oxidising alcohols to make aldehydes and ketones

An aldehyde is an organic compound containing a formyl group. The formyl group is a functional group, with the structure R-CHO, consisting of a carbonyl center (a carbon double bonded to oxygen) bonded to hydrogen and an R group, which is any generic alkyl or side chain. The group without R is called the aldehyde group or formyl group. Aldehydes differ from ketones in that the carbonyl is placed at the end of a carbon skeleton rather than between two carbon atoms. Aldehydes are common in organic chemistry. Many fragrances are aldehydes. CDH offers many products in Aldehyde & Derivatives available in different grade of purity.


Nomenclature of Aldehydes and Ketones

In other words, if you start from a primary alcohol, you will get an aldehyde.

IUPAC Nomenclature for Aldehydes and Ketones
For the IUPAC nomenclature, the longest continuous carbon chain is the parent compound. Number the chain so that the C-O or bond has the lowest possible number. Give the location of the C-O bond with a number for ketones. From the alkyl prefixes, use Aanal@ for aldehydes, and Aanone@ for ketones. Name and number substituents.


Synthesis of Aldehyde-Linked Nucleotides and DNA and …

Yeast and several other microorganisms undergo glycolysis or fermentation to produce ethanol from sugars. This is the process to make wine, beer, and other alcoholic products from grains and fruits.
The reactions of glycolysis are identical to those described up to the production of pyruvic acid. The difference is in the fate of pyruvic acid. In fermentation, pyruvic acid is converted first to ethanal (acetaldehyde) and then to ethanol. In the second step, the NADH from Step 5 is converted back to NAD+ in this process. The NADH supplies the hydrogen for the reduction of the ethanal (an aldehyde) into ethanol (an alcohol).

Ketone synthesis from aldehyde? | Yahoo Answers

Background for Aldehydes and Ketones
An aldehyde contains at least one hydrogen attached to the C of a C=O (carbonyl group). A ketone contains two alkyl groups attached to the C of the carbonyl group. The carbon in the carbonyl is sp2 hybridized, has a bond angle of 120o, and is trigonal planar. Aldehydes and ketones have dipole-dipole attractions between molecules, and no hydrogen bonding between molecules. These compounds can hydrogen bond with compounds have O-H or N-H bonds. The melting points and boiling points of aldehydes and ketones are between alkanes and alcohols. Small aldehydes and ketones are soluble in water. Some compounds are very flammable.

Oxime synthesis - how to convert/remove unreacted aldehyde?

use an excess of the alcohol. That means that there isn't enough oxidising agent present to carry out the second stage and oxidise the aldehyde formed to a carboxylic acid.

Synthesis of peptide aldehydes - Moulin - 2006 - …

The following problems review many aspects of aldehyde and ketone chemistry. The first three questions concerns their nomenclature. The fourth also requires knowledge of nomenclature, together with simple chemical properties.. The fifth question asks you to match descriptions with corresponding structures. The sixth reviews oxidation-reduction terminology. The seventh examines three common reactions as applied to eight carbonyl compounds. You should only be concerned with the aldehyde and ketone reactants. The eighth question asks you to select those reactions, among a large group, that would yield aldehyde or ketone products. The next question focuses on possible reactions of a simple aldehyde. The tenth illustrates three ways questions about chemical reactions may be formulated. The eleventh and twelfth questions require you to draw the structural formulas for the products of many aldehyde and ketone reactions. Next, two questions about the mechanism of acetal and enamine formation are given. Finally, the last question concerns the aldol condensation.