Structure of Aldehydes and Ketones
Aldehydes and ketones incorporate a carbonyl functional group, C=O. These are organic compounds with structures -CHO and RC(=O)R’ where R and R’ represent carbon-containing substituents respectively. Aldehydes and Ketones are often called as methanoyl or formyl group. The carbon atom of this group has 2 remaining bonds that might be occupied by aryl or alkyl or substituents. If neither of these substituents is hydrogen, the compound is a Ketone. If at least one is hydrogen, the compound is an Aldehyde.
In aldehydes, the carbonyl group has one hydrogen atom attached to it together with either a 2nd hydrogen atom or a hydrogen group which may be an alkyl group or one containing a benzene ring.
Example:
One can notice that all these have the exact same end to the molecule. The only difference is the complexity of the other attached group.
In ketones, the carbonyl group has 2 hydrocarbon groups attached to it. These can be either the ones containing benzene rings or alkyl groups. Ketone does not have a hydrogen atom attached to the carbonyl group.
Example:
Propane is generally written as CH3COCH3. In pentanone, the carbonyl group could be in the middle of the chain or next to the end – giving either pentan-3-one or pentan-2-one.
Combined with other functional group aldehydes and ketone are widespread in nature. Compounds such as cinnamaldehyde (cinnamon bark), vanillin (vanilla bean), Citra (lemongrass), helminthosporal (a fungal toxin), carvone (spearmint and caraway), camphor (camphor trees) are found chiefly in microorganisms or plants. Whereas, compounds such as muscone (musk deer), testosterone (male sex hormone), progesterone (female sex hormone), cortisone (adrenal hormone) have animal and human origin.
Formaldehyde is the simplest aldehyde whereas acetone is the smallest ketone. There are a number of aldehydes and ketones which find application due to their chemical properties. Some uses of Aldehydes and Ketones are discussed in the points below.
Aldehydes and Ketones are obtained from products of many reactions. Some reactions for the synthetic preparation of Aldehyde and Ketone is mention below.