# 11.12 A Summary of Reactivity: $$S_{N}1$$, $$S_{N}2$$, E1, E1cB, and E2

Objectives

After completing this section, you should be able to

1. determine whether a specified substrate is most likely to undergo an E1, E2, SN1 or SN2 reaction under a given set of conditions.
2. describe the conditions under which a given substrate is most likely to react by a specified mechanism (E1, E2, SN1 or SN2).

Study Notes

This section summarizes much of what has been discussed in the chapter. It focuses on how a given substrate will behave under certain conditions, but does not deal with the stereochemistry of the products.

### Content

Having discussed the many factors that influence nucleophilic substitution and elimination reactions of alkyl halides, we must now consider the practical problem of predicting the most likely outcome when a given alkyl halide is reacted with a given nucleophile. As we noted earlier, several variables must be considered, the most important being the structure of the alkyl group and the nature of the nucleophilic reactant.In general,  in order for an SN1 or E1 reaction to occur, the relevant carbocation intermediate must be relatively stable.  Strong nucleophile favor substitution, and strong bases, especially strong hindered bases (such as tert-butoxide) favor elimination.

The nature of the halogen substituent on the alkyl halide is usually not very significant if it is Cl, Br or I. In cases where both SN2 and E2 reactions compete, chlorides generally give more elimination than do iodides, since the greater electronegativity of chlorine increases the acidity of beta-hydrogens. Indeed, although alkyl fluorides are relatively unreactive, when reactions with basic nucleophiles are forced, elimination occurs (note the high electronegativity of fluorine).

The following table summarizes the expected outcome of alkyl halide reactions with nucleophiles. It is assumed that the alkyl halides have one or more beta-hydrogens, making elimination possible; and that low dielectric solvents (e.g. acetone, ethanol, tetrahydrofuran & ethyl acetate) are used. When a high dielectric solvent would significantly influence the reaction this is noted in red. Note that halogens bonded to sp2 or sp hybridized carbon atoms do not normally undergo substitution or elimination reactions with nucleophilic reagents.

 Nucleophile Alkyl Group Primary RCH2– Anionic Nucleophiles ( Weak Bases: I–, Br–, SCN–, N3–, CH3CO2– , RS–, CN– etc. ) pKa's   from -9 to 10 (left to right) Anionic Nucleophiles ( Strong Bases: HO–, RO– ) pKa's   > 15 Neutral Nucleophiles ( H2O, ROH, RSH, R3N ) pKa's  ranging from -2 to 11 Rapid SN2 substitution. The rate may be reduced by substitution of β-carbons, as in the case of neopentyl. Rapid SN2 substitution. E2 elimination may also occur.  e.g. ClCH2CH2Cl + KOH ——> CH2=CHCl SN2 substitution. (N ≈ S >>O) SN2 substitution and / or E2 elimination (depending on the basicity of the nucleophile). Bases weaker than acetate (pKa = 4.8) give less elimination. The rate of substitution may be reduced by branching at the β-carbons, and this will increase elimination. E2 elimination will dominate. SN2 substitution. (N ≈ S >>O) In high dielectric ionizing solvents, such as water, dimethyl sulfoxide & acetonitrile, SN1 and E1 products may be formed slowly. E2 elimination will dominate with most nucleophiles (even if they are weak bases). No SN2 substitution due to steric hindrance. In high dielectric ionizing solvents, such as water, dimethyl sulfoxide & acetonitrile, SN1 and E1 products may be expected. E2 elimination will dominate. No SN2 substitution will occur. In high dielectric ionizing solvents SN1 and E1 products may be formed. E2 elimination with nitrogen nucleophiles (they are bases). No SN2 substitution. In high dielectric ionizing solvents SN1 and E1 products may be formed. Rapid SN2 substitution for 1º and 2º-halides. For 3º-halides a very slow SN2 substitution or, if the nucleophile is moderately basic, E2 elimination. In high dielectric ionizing solvents, such as water, dimethyl sulfoxide & acetonitrile, SN1 and E1 products may be observed. Rapid SN2 substitution for 1º halides. E2 elimination will compete with substitution in 2º-halides, and dominate in the case of 3º-halides. In high dielectric ionizing solvents SN1 and E1 products may be formed. Nitrogen and sulfur nucleophiles will give SN2 substitution in the case of 1º and 2º-halides. 3º-halides will probably give E2 elimination with nitrogen nucleophiles (they are bases). In high dielectric ionizing solvents SN1 and E1 products may be formed. Water hydrolysis will be favorable for 2º & 3º-halides. Rapid SN2 substitution for 1º and 2º-halides. For 3º-halides a very slow SN2 substitution or, if the nucleophile is moderately basic, E2 elimination. In high dielectric ionizing solvents, such as water, dimethyl sulfoxide & acetonitrile, SN1 and E1 products may be observed. Rapid SN2 substitution for 1º halides (note there are no β hydrogens). E2 elimination will compete with substitution in 2º-halides, and dominate in the case of 3º-halides. In high dielectric ionizing solvents SN1 and E1 products may be formed. Nitrogen and sulfur nucleophiles will give SN2 substitution in the case of 1º and 2º-halides. 3º-halides will probably give E2 elimination with nitrogen nucleophiles (they are bases). In high dielectric ionizing solvents SN1 and E1 products may be formed. Water hydrolysis will be favorable for 2º & 3º-halides.

### Exercises

#### Questions

Q11.12.1

Label the following reactions as SN1, SN2, E1, or E2.

S11.12.1

A – SN2

B – E1

C – SN1

D – E2