Reactions of Alkyl Halides-1

Reactions of Alkyl Halides
1. GRIGNARD REAGENT
Alkyl halides, RX, react with magnesium metal in ether
solvent to yield alkylmagnesium halides, RMgX. The
products, called Grignard reagents after their
discoverer, Victor Grignard, are examples of
organometallic compounds because they contain a
carbon–metal bond
Alkenyl (vinylic) and aryl (aromatic) halides also react
with magnesium to give Grignard reagents. The
halogen can be Cl, Br, or I, but not F.
Alkenyl (vinylic) and aryl (aromatic) halides also react
with magnesium to give Grignard reagents. The
halogen can be Cl, Br, or I, but not F.
A Grignard reagent is formally the magnesium salt,

R3C+- MgX, of a carbon acid, R3COH, and is thus a
carbon anion, or carbanion.
Grignard reagents must therefore be protected from
atmospheric moisture to prevent their being
protonated and destroyed in an acid–base reaction:
R - Mg - X + H2O  R- H + HO – Mg – X
Grignard reagents themselves don’t occur in

living organisms, but they are useful carbon-
based nucleophiles in important laboratory
reactions.
2.Nucleophilic Substitution Reactions
Because they are electrophiles, alkyl halides do
one of two things when they react with
nucleophiles/bases, such as hydroxide ion:
either they undergo substitution of the X group
by the nucleophile or elimination of HX to yield
an alkene.
Each step involves the substitution of one
nucleophile (chloride ion, Cl-, or hydroxide ion,
OH-) by another.
Example 2
Predicting the Product of a Substitution Reaction
What is the substitution product from reaction of 1-
chloropropane with NaOH?
Strategy
Write the two reactants, and identify the nucleophile
(in this instance, OH-)and the leaving group (in this
instance, Cl+). Then, replace the -Cl group by -OH and
write the complete equation.
Example 3
Using a Substitution Reaction in a Synthesis
How would you prepare propane-1-thiol,
CH3CH2CH2SH, using a nucleophilic substitution
reaction?
Strategy
Identify the group in the product that is introduced by
nucleophilic substitution.
In this case, the product contains an - SH group, so it
might be prepared by reaction of SH- (hydrosulfide ion)
with an alkyl halide such as 1-bromopropane
3. SUBSTITUTION, SN2 Reaction
Example 4
Predicting the Product of a Substitution Reaction
What product would you expect to obtain from the SN2
reaction of (S)-2-iodooctane with sodium cyanide, NaCN?
Strategy
Identify the nucleophile (cyanide ion) and the leaving
group (iodide ion). Then carry out the substitution,
inverting the configuration at the chirality center.
(S)-2-Iodooctane reacts with CN- to yield (R)-2-
methyloctanenitrile.
Steric Effects in SN2 Reactions
The ease with which a nucleophile can approach a
substrate to carry out an SN2 reaction depends on steric
accessibility to the halide-bearing carbon. Bulky
substrates, in which the halide-bearing carbon atom is
difficult to approach, react much more slowly than
those in which the carbon is more accessible
Example 5
Predicting the Rates of Substitution Reactions
Which would you expect to be faster, the SN2 reaction
of OH- ion with 1-bromopentane or with 2-
bromopentane?
Strategy
Decide which substrate is less hindered. Since 1-
bromopentane is a 1° halide and 2-bromopentane is a
2° halide, reaction with the less hindered 1-
bromopentane is faster
4.SUBSTITUTION, SN1 Reaction
SN1 reactions take place only on tertiary substrates and
only under neutral or acidic conditions in a hydroxylic
solvent such as water or alcohol.
R-Br + H2O  R-OH + HBr
Example 6:Predicting the Stereochemistry of a
Substitution Reaction
What stereochemistry would you expect for the SN1
reaction of (R)-3-bromo-3-methylhexane with
methanol to yield 3-methoxy-3-methylhexane?
Strategy
First draw the starting alkyl halide, showing its
correct stereochemistry. Then replace the -Br with a
methoxy group ( - OCH3) to give the racemic product.
5.ELIMINATIONS, E2 Reaction
According to Zaitsev’s rule, a predictive guideline

formulated in 1875 by the Russian chemist Alexander
Zaitsev, base-induced elimination reactions generally
give the more highly substituted alkene product—that
is, the alkene with the larger number of alkyl
substituents on the double bond.
Treatment of 2-bromobutane with KOH in ethanol, for
instance, gives primarily but-2-ene (disubstituted; two
alkyl group substituents on the double-bond
ZAITSEV’S RULE In the elimination of HX from an

alkyl halide, the more highly substituted alkene
product predominates
Example.7 Predicting the Product of an Elimination
Reaction
What product would you expect from reaction of 1-
chloro-1-methylcyclohexane with KOH in ethanol?
Strategy Treatment of an alkyl halide with a strong
base such as KOH yields an alkene.
To find the products in a specific case, draw the
structure of the reactant and locate the hydrogen
atoms on neighboring carbons. Then generate the
potential alkene products by removing HX in as many
ways as possible. The major product will be the one
that has the most highly substituted double bond—in
this case, 1-methylcyclohexene
6.ELIMINATIONS E1 AND E1cBReactions

Reactions of Alkyl Halides-1

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Reactions of Alkyl Halides

A Grignard reagent is formally the magnesium salt,

Grignard reagents themselves don’t occur in

According to Zaitsev’s rule, a predictive guideline

ZAITSEV’S RULE In the elimination of HX from an

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