Presentation on theme: "Electrophilic Aromatic Substitution Activating and Directing effects of substituents already on the ring."— Presentation transcript:
Electrophilic Aromatic Substitution Activating and Directing effects of substituents already on the ring
Products of Nitration 1 hr 48 hr 0.0003 hr
Mechanism of Electrophilic Aromatic Substitution With a substituent group G Depending on the nature of the substituent, the substituent G may stabilize the carbocation intermediate and therefore speed the reaction, or it may raise the energy of the carbocation and slow the reaction. Substituents that make the ring react faster (than benzene) with electrophiles are called activators; those that make the ring react slower (than benzene) are called deactivators.
Substituent effects All activators also direct incoming electrophiles to the ortho- and the para- positions. Most deactivators direct incoming electrophiles to the meta position. The exceptions are the halogens, which are weakly deactivating yet ortho-para directing.
Classification of Substituents
Product Distribution in Nitration (Percent %) (Percent %) X ortho meta paraX ortho meta para (meta-directing Deactivators) (ortho- and para-directing Deactivators) -N(CH 3 ) 3 289 11-F 13 1 86 -NO 2 7912-Cl 35 1 64 -CO 2 H22772-Br 43 1 56 -CN17812-I 45 1 54 -CO 2 CH 2 CH 3 28722 (ortho- and para-directing Activators) -COCH 3 26722-CH 3 63 3 34 -CHO19729-OH 50 0 50 -NHCOCH 3 19 2 79
o,p-Activators (alkyl & aryl groups) 3º, especially stable
o,p-Activators with a lp of electrons 4 resonance forms o- m- p-
o,p-Deactivators (Halogens) 4 resonance forms o- m- p-
meta-directing Deactivators Especially UNSTABLE** o- m- p-
Explanation of meta- deactivators Meta directors slow the reaction by raising the energy of the carbocation intermediate because they have (in one resonance form, shown below) a positively charged atom attached to the ring. Two positively charged atoms so close together is very high in energy (especially unstable). nitro group sulfonic acid ketone nitrile
Summary of Substituent Effects When the substituent is R (alkyl) or Ar (aryl), the resonance hybrid cation intermediate has three resonance forms. For attack of the electrophile at the ortho or para positions, one of these is a 3º carbocation, which is especially stable. This lowers the energy of the intermediate, thus facilitates (speeds) the substitution reaction at the o- and p- positions. When the substituent has a lone pair of electrons, such as the halogens, oxygen or nitrogen, the resonance hybrid for attack of the electrophile at the ortho and para positions has four resonance forms. This lowers the energy of the those intermediates, thus facilitates (speeds) the substitution reaction at the o- and p- positions.
Summary of Substituent Effects… When the substituent has a multiple bond conjugated with the ring, and the second atom from the ring is more electronegative than the first, the substituent deactivates the ring and directs incoming electrophiles meta. It does this by raising the energy of the carbocation intermediates from ortho and para attack by an electrophile even more than it raises the energy of the intermediate resulting from meta attack.
Additivity of substituent effects in disubstituted aromatic rings Rule 1: If the directing effects of two substituents reinforce each other, the predicted product predominates. (o,p) (m)
Additivity of substituent effects… Rule 2: If the directing effects of two substituents oppose each other, the more activating group dominates, but mixtures often result. (o,p; STRONG activator) (o,p; weak activator)
Additivity of substituent effects… Rule 3: Substitution almost never occurs between two substituents meta to each other. (o,p) X (too crowded)
Additivity of substituent effects… Rule 4: With a bulky o,p- director and/or a bulky electrophile, para substitution predominates. (o,p; BULKY) (HSO 3 + is a BULKY electrophile)