The correct IUPAC name for CH3CH2Br is Bromoethane, as it consists of a two-carbon chain with a bromine substituent.

The compound CH3CH2OH is an alcohol with two carbon atoms, which is named ethanol.

The longest carbon chain has four carbons, and the bromine is attached to the second carbon, making the IUPAC name 2-bromobutane.

The longest carbon chain contains 5 carbons with a double bond at the first carbon, making it 1-pentene.

The compound CH3-CH2-NH2 is named ethylamine according to IUPAC nomenclature.

The product is benzene sulfonic acid, formed by the addition of a sulfonyl group to the benzene ring.

The compound formed is acetophenone, which results from the acetylation of phenol.

Bromination of phenol typically occurs at the ortho or para positions, with 2-bromophenol being one of the major products.

The compound C3H6O can be identified as a ketone, specifically Propan-2-one, which has the carbonyl group on the second carbon.

The compound with the formula C4H10O and a branched structure is 2-Butanol, which has the hydroxyl group (-OH) on the second carbon.

The compound with the formula C4H9Br is 1-bromobutane, as it is a straight-chain brominated alkane.

The compound is a ketone with five carbon atoms. The longest carbon chain is pentane, and the ketone group is on the second carbon, making it 2-Pentanone.

The compound C5H10O can be a ketone, and the longest carbon chain with the carbonyl group is 5 carbons long, making it 2-Pentanone.

The compound C5H12 is an alkane with five carbon atoms, which is named pentane.

The correct IUPAC name is phenylacetic acid, as it has a phenyl group attached to the acetic acid structure.

The compound is acetophenone, which consists of a phenyl group attached to a carbonyl group and a methyl group.

The correct IUPAC name is phenylacetic acid, as it contains a phenyl group attached to an acetic acid moiety.

The IUPAC name of C6H5CH2OH is benzyl alcohol, which consists of a benzene ring attached to a -CH2OH group.

The IUPAC name of C6H5NO2 is nitrobenzene, which contains a nitro group (-NO2) attached to a benzene ring.

The longest carbon chain contains 4 carbons, and the aldehyde group is at the end, making it 3-methylbutanal.

The longest carbon chain has four carbons, and the bromine is on the first carbon, making it 1-bromo-3-methylbutane.

The longest carbon chain has five carbons, and the methyl group is on the third carbon, making it 3-methylpentane.

The complex has a cobalt ion in the +3 oxidation state, and the correct IUPAC name is Pentaamminechlorocobalt(III) chloride.

The correct IUPAC name is phenylacetic acid, as it consists of a phenyl group attached to an acetic acid moiety.

The compound is a carboxylic acid with a methyl group on the second carbon, making it 2-methylbutanoic acid.

The longest carbon chain has 4 carbons (butane) with a methyl group on the second carbon, making it 2-methylbutane.

The correct IUPAC name is 1-bromo-2-methylpropane, as the longest carbon chain has three carbons and the bromine is on the first carbon.

The correct IUPAC name is 1-Methyl-2-nitrobenzene, indicating the positions of the substituents on the benzene ring.

The correct IUPAC name is Hexaammine chromium(III) chloride, where 'ammine' indicates the ammonia ligands and chromium is in the +3 oxidation state.

HPLC offers higher resolution and speed due to the use of high pressure to push solvents through the column, allowing for better separation of components.