Alcohols have higher boiling points than ethers and alkanes due to hydrogen bonding.

The compound is Butan-2-ol, as the hydroxyl group is on the second carbon.

The compound CH3CH2CH2OH is named butan-1-ol as it has four carbon atoms and the hydroxyl group is on the first carbon.

The compound CH3CH2OCH2CH3 is named diethyl ether, as it consists of two ethyl groups bonded to an oxygen atom.

Oxidation of a primary alcohol typically leads to the formation of a carboxylic acid.

Dehydration of alcohols typically yields alkenes through elimination reactions.

Depending on the type of alcohol, oxidation with potassium dichromate can yield aldehydes, ketones, or carboxylic acids.

Dehydration of ethanol typically yields ethylene (ethene) as the main product.

Phenol reacts with bromine water to form 2,4,6-tribromophenol, a white precipitate.

Zinc dust reduces phenol to benzene.

Phenol reacts with bromine water to form 2,4,6-tribromophenol, a white precipitate.

The conversion of alcohols to alkyl halides typically involves a nucleophilic substitution reaction.

Dehydration of ethanol leads to the formation of ethylene (ethene) by elimination of water.

Phenol reacts with bromine water to form 2,4,6-tribromophenol, a white precipitate.

Phenol reacts with bromine to form bromophenol, which is a substitution reaction.

The reaction of an alcohol with a carboxylic acid produces an ester through a process called esterification.

Isopropanol (2-propanol) is a secondary alcohol, as the hydroxyl group is attached to a carbon that is connected to two other carbons.

The reaction between an alcohol and an acid to form an ether is a condensation reaction.

Phenol reacts with sodium hydroxide in a nucleophilic substitution reaction to form phenoxide ion.

The reaction of phenol with sodium metal leads to the formation of biphenyl through the Wurtz reaction.

Butan-1-ol has the highest boiling point due to its longer carbon chain and stronger hydrogen bonding.

Methanol is the most acidic among the given alcohols due to the absence of steric hindrance.

Methanol is the most acidic among the given alcohols due to its smaller size and higher electronegativity.

2-butanol can be oxidized to form a ketone, specifically butanone.

Phenol is an aromatic compound with a hydroxyl group directly attached to a benzene ring.

Diethyl ether is well-known for its use as a general anesthetic in the past.

Phenols are weakly acidic due to the presence of the hydroxyl group attached to the aromatic ring.

Alcohols undergo esterification when they react with carboxylic acids to form esters.

Ethers undergo nucleophilic substitution reactions under strong acidic conditions.

Phenols undergo electrophilic substitution reactions due to the presence of the hydroxyl group, which activates the benzene ring.