Carbonyls (as in 4 and 5) are always electron withdrawing due to the Oxygen's electronegativity. Similarly, the oxygens on the nitrate (1) are electron withdrawing.

A tert-butyl functional group is electron donating and will therefore activate the ortho and para positions. However, the ortho positions are sterically hindered by the bulky tert-butyl group. Therefore, the para position will be favored.

is the only electron-withdrawing substituent because it contains two electronegative oxygen atoms which pull electrons from the benzene ring towards itself. This effect is electron-withdrawing and makes the ring slightly positive in charge. All the other substituents are electron-donating groups, which activate the ring for electrophilic addition.

is the only electron-donating group listed. Therefore, it will add to the ortho and para positions on phenol. The rest of the substituents are highly electron-withdrawing groups and will add to the meta positions on phenol.

Several resonance structures can be drawn for the molecule nitrobenzene. These are shown below.

From these resonance structures, an overall molecular electronic distribution can be determined:

Because the overall charge distribution puts partial positive charges on carbons , , and , these carbons have an increased electrophilic character. Therefore, these carbons are less likely than the other carbons to accept an incoming electrophilic substituent, making these positions less likely to be substituted. By default, carbons , and , known as the meta positions are the only ones nucleophilic enough to carry out this reaction.

In the molecule shown, the aldehyde group will direct incoming substituents to positions meta to it, and both the the hydroxyl group AND the fluorine group will direct incoming substituents to positions ortho or para to them. Options I and III show the incoming substituent meta to the aldehyde group, as well as either ortho or para to both the fluorine group and hydroxyl group. Therefore, they are both possible products.

Note: because option III shows attachment at a carbon that is slightly less sterically hindered than that of option I, option III will be produced in a slightly greater quantity.

The reagents shown will add a bromine to an aromatic ring through an electrophilic aromatic substitution mechanism. A nitro group is a strong electron withdrawing group and a benzene deactivator. All benzene deactivators (with the exception of halogens) direct incoming substituents to the meta positions. Therefore, option III is the major product.

Several resonance structures can be drawn for the molecule phenol. These are shown below.

Because the overall charge distribution puts partial negative charges on carbons , , and , these carbons have an increased nucleophilic character. Therefore, these carbons are more likely than the other carbons to accept an incoming electrophilic substituent, making these positions more likely to be substituted. Carbons and are known as the ortho positions, and carbon is known as the para position.

Phenol contains the hydroxide group, which is an electron donor, puts electron density into the benzene ring. Resonance structures are drawn as follows

With the exception of halogens, meta directors deactivate a benzene ring. In other words, they make the benzene ring less reactive, especially in an electrophilic aromatic substitution (EAS) reaction. Meta directors have little electron density at the point of contact with the benzene ring. For example, a carboxylic acid is a meta director because it experiences resonance, a delocalization of electrons. All of the answer choices in this problem have a lone pair of electrons on the point of contact with the benzene ring and they all are ortho/para directors.