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Hydrocarbons

Question
CBSEENCH11007755

How are alkanes formed from alkyl halides?

Solution

Preparation from alkyl halides. Alkanes can be prepared from alkyl halides by the following methods:
1. By Wurtz’s reaction. It involves the chemical reaction between an alkyl halide and metallic sodium in the presence of dry ether. Two molecules of alkyl halide will react to form higher alkanes.
stack straight R minus straight X with Alkyl space halide below space plus space 2 Na space plus space stack straight X minus straight R with Alkyl space halide below space space rightwards arrow with Dry space ether on top space space stack straight R space minus space straight R with Alkane below space plus space 2 NaX
stack CH subscript 3 minus straight I with Methyl space iodide below space plus space 2 Na space plus space straight I minus CH subscript 3 space rightwards arrow with Dry space ether on top space space stack CH subscript 3 space minus CH subscript 3 with Ethane below space plus space 2 NaI
    stack straight C subscript 2 straight H subscript 5 Br with Ethyl space bromide below space plus space 2 Na space plus space stack Br space minus space straight C subscript 2 straight H subscript 5 with Ethyl space bromide below space space rightwards arrow with Dry space ether on top space stack straight C subscript 2 straight H subscript 5 space minus space straight C subscript 2 straight H subscript 5 with straight n minus Butane below space space plus space 2 NaBr
Methane cannot be prepared by this method. 
When we use mixed alkyl halides, for example, methyl bromide and ethyl bromide, more than one product are obtained. 
stack CH subscript 3 space minus Br with Methyl space bromide below space plus space 2 Na space plus space stack Br space minus space straight C subscript 2 straight H subscript 5 with Ethyl space bromide below space rightwards arrow with Dry space ether on top space stack CH subscript 3 space minus space straight C subscript 2 straight H subscript 5 with Propane below space plus space 2 Nal
stack CH subscript 3 space minus space Br with Methyl space bromide below space plus space 2 Na space plus space stack Br space minus space CH subscript 3 with Methyl space bromide below space rightwards arrow with Dry space ether on top space stack CH subscript 3 with Ethane below space minus space CH subscript 3 space plus space 2 NaBr
stack straight C subscript 2 straight H subscript 5 space minus Br with Ethyl space bromide below space plus space 2 Na space plus space stack Br minus straight C subscript 2 straight H subscript 5 with Ethyl space bromide below space rightwards arrow with Dry space ether on top space space stack straight C subscript 2 straight H subscript 5 with straight n minus Butane below space minus space straight C subscript 2 straight H subscript 5 space plus space 2 NaBr
This reaction is not suitable to prepare pure alkane with an odd number of carbon atoms because of side reactions.

Mechanism of Wurtz’s reaction: Two different mechanisms have been proposed.
(a) Intermediate formation of an organometallic compound:
straight R space minus space straight X space plus space 2 Na space rightwards arrow space stack straight R space minus space Na with stack Alkyl space sodium with left parenthesis Intermediate right parenthesis below below space plus space NaX
straight R space minus straight X space plus space RNa space rightwards arrow space stack straight R space minus space straight R with Alkane below space plus space Nax
(b) Intermediate formation of free radical:
straight R space minus space straight X space plus space Na space space rightwards arrow space space space straight R with. on top space plus space Na to the power of plus straight X to the power of minus
space space space straight R with. on top space plus space straight R with. on top space space rightwards arrow space space stack straight R space minus space straight R with Alkane below
2. By Corey-House reaction: By Corey-House reaction: An alkyl halide is first treated with lithium metal in dry ether to form alkyl lithium. This then reacts with cuprous iodide to yield lithium dialkyl copper and which on subsequent treatment with a suitable alkyl halide gives the desired alkane.

(R and R' may be same or different alkyl groups)

For example:

This reaction is very useful for the preparation of both symmetrical and unsymmetrical alkanes.
3. By the reduction of alkyl halides: The reduction of alkyl halide is carried:
(i) With zinc-copper and alcohol or zinc and HCl or zinc and NaOH: Zinc reacts with alcohol to produce nascent hydrogen which brings about reduction.


(ii) By catalytic reduction: By using hydrogen gas in the presence of platinum or palladium.
straight C subscript 2 straight H subscript 5 Br space plus space straight H subscript 2 space rightwards arrow from Heat to Pt space or space Pd of space stack straight C subscript 2 straight H subscript 6 with Ethane below space plus space HBr
stack CH subscript 3 CH subscript 2 CH subscript 2 Cl with straight n minus Propyl space chloride below space plus space straight H subscript 2 space rightwards arrow with Pd on top space CH subscript 3 space minus stack space CH subscript 2 space minus space CH subscript 3 with Propane below space plus space HCl
(iii) With red phosphorus and hydrogen iodide:
stack straight C subscript 2 straight H subscript 5 Br space with Ethyl space bromide below plus space 2 HI space rightwards arrow from straight P to 420 space straight K of space straight C subscript 2 straight H subscript 6 space plus space HBr space plus space straight I subscript 2
stack straight C subscript 2 straight H subscript 5 minus straight I with Ethyl space iodide below space plus space HI space rightwards arrow from straight P to 420 space straight K of space straight C subscript 2 straight H subscript 6 space plus space straight I subscript 2

The function of red phosphorus is to combine with iodine to form phosphorus tri-iodide PI3. If it is not done, iodine will react back with an alkane to form alkyl halide.
4. Through the formation of Grignard reagent: Alkyl halides react with dry magnesium metal in the presence of anhydrous ether to form alkyl magnesium halides, also called Grignard reagent.
CH subscript 3 CH subscript 2 Br space plus space Mg space rightwards arrow with Dry space ether on top space stack CH subscript 3 CH subscript 2 MgBr with Ethyl space magnesium space bromide below
Grignard reagent can be easily decomposed by water or alcohol to form alkane.