IUPAC Naming of Aldehydes and Ketones

The carbon atom of the ring to which the aldehyde –C is attached to will get the # ______ location in naming the ring.

For open-chain ketones, numbering begins at the end nearer the ______ carbon.

The parent name of an open-chain ketone is derived by replacing the terminal –______ of the corresponding alkane name with suffix –one.

If an aldehyde group (-CHO) is present in the molecule, the ketone group (=O) becomes a ______ substituent.

For cyclic ketones, the carbonyl C (C=O) is always numbered as ______.

The parent name of a cyclic ketone is derived by replacing the ending –______ of the corresponding cycloalkane with suffix –one.

For mixed ethers, the shorter alkyl groups becomes the ______ substituents while the longer alkyl groups becomes the alkane parent.

According to IUPAC naming conventions, the parent chain must contain the ______ group and the aldehyde –C is numbered as C-1.

The parent name is derived by simply replacing the terminal –e of the corresponding alkane name with suffix ______.

For cyclic aldehydes in which the –CHO group is directly attached to a ring, the suffix ______ is added to the name of the ring.

Select the parent chain containing the __________ group and derive the parent name by replacing the ending of the corresponding alkane with -ol.

In Williamson Ether Synthesis, the ether part is considered an ______ substituent.

In IUPAC naming conventions, the shorter alkyl group becomes the ______ while the longer alkyl group becomes the alkane parent.

The __________ directly attached to a benzene ring is a Phenol compound.

Write the name in one word, and if the compound has more than 1 __________ group, use the prefixes di-, tri-, tetra-, so forth.

Begin numbering at the end nearer the __________ group.

If the compound has more than 1 __________ groups, use the prefixes di-, tri-, tetra-, so forth.

Number the substituents according to their position on the alkane chain and the position of the __________ group is also indicated.