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

The longest chain has 4 carbons with a carboxylic acid group, making it 2-methylbutanoic acid.

The correct IUPAC name for CH3-CH2-CH(CH3)-OH is 2-Methyl-1-propanol, as the longest chain has three carbons and the hydroxyl group is on the first carbon.

The longest carbon chain has four carbons and the hydroxyl group is on the first carbon, making it Butan-1-ol.

C5H10 is a saturated hydrocarbon, which is pentane.

The longest carbon chain has four carbons, and the methyl group is on the second carbon, making it 2-Methylbutanoic acid.

The compound is 2-methylbutanoic acid, as the carboxylic acid is on the second carbon of the butane chain.

The longest carbon chain has four carbons with an aldehyde group, making it 2-Methylbutanal.

The longest chain has four carbons, and there is a methyl group on the second carbon, making it 2-methylbutane.

The longest chain has five carbons (pentane) with two methyl groups on the third carbon, making it 3,3-dimethylpentane.

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

The compound has three carbon atoms in the longest chain and a carboxylic acid functional group, making it propanoic acid.

The critical point of a gas is the temperature and pressure at which it can no longer be liquefied, regardless of the pressure applied.

The -CF3 group is a strong electron-withdrawing group, making the aromatic ring less reactive in electrophilic substitution.

The methoxy group (-OCH3) is an activating group and directs electrophilic substitution to the ortho and para positions.

A nitro group is a strong electron-withdrawing group that deactivates the benzene ring, making it less reactive towards electrophilic substitution.

A nitro group is a strong electron-withdrawing group that deactivates the benzene ring towards electrophilic substitution.

Strong electron-donating groups increase the electron density of the aromatic ring, enhancing its reactivity towards electrophiles.

A strong electron-withdrawing group decreases the reactivity of the benzene ring in electrophilic substitution by destabilizing the sigma complex.

Increasing the number of alkyl groups generally increases the basicity of amines due to the electron-donating effect.

Increasing the number of gas molecules in a container at constant volume increases the frequency of collisions with the walls, thus increasing pressure.

Physisorption typically decreases with increasing temperature because the kinetic energy of the molecules increases, overcoming the weak van der Waals forces.

The electron configuration of chlorine (atomic number 17) is 1s2 2s2 2p6 3s2 3p5.

The reaction of 1-chloropropane with potassium tert-butoxide favors elimination, leading to the formation of propene as the major product.

Hydroboration-oxidation of 1-butyne leads to the formation of 2-butanol due to anti-Markovnikov addition.

The strong base facilitates the E2 elimination, resulting in the formation of 2-methylpropene.

Hydroboration-oxidation of 2-methylpropene leads to the formation of 2-methylpropan-1-ol due to anti-Markovnikov addition of water.

Chlorosulfonic acid introduces a sulfonyl group at the para position due to the activating effect of the methoxy group.

The expected product is para-bromoanisole, as the methoxy group is an electron-donating group that directs electrophilic substitution to the para position.

The expected product is 2,4,6-tribromophenol, as phenol is highly reactive towards electrophilic substitution due to the hydroxyl group.