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.Φ>' cw# CH2=C-CH2C1

— REACTS READIIY THROUGH BOTH ITS Cl ATOM AND DOUBU BOND Wé-.

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Illpie^WitiliS' AVAILABLE m COMMIitClÂl QUANTITIES

The reactions of this important compound are characterized by rapidity and freedom from by-products· Reylacement of the chlorine atom leads to a variety of compounds having widely different structures. The double bond can be reacted with a variety of reagents to give products useful for the further synthesis of a large number of chemicals, pharmaceuticals and anaesthetics.

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The following are examples of replacement and double bond reactions :

PHYSICAL Specific Grotty Qi2Q ,. 0^

CH2 = CH-CH2C1 Br2-AareofropfcOcta

CH2Br-CHBi-CH2Cl {1-chloro-2,3-dibromopropane)

CH2 = CH-CH2C1 + CuCN * CH2=CH-CH2CN + CuCl

(allyl cyanide)

CH2=CH-CH2C1 + NaOR -CH,=CH-CH2OR + NaCI

(alkyl allyl ether)

Refi ractive index, N„ 20

44.9°c

12* 5'Wnjtafctfj|g-97il*-

1.4Î5I c°n:poMM''

Other Shell Chemical products include : Allyl Alcohol, Cyclohexane, Diisobutylene, Acetone and Methyl Ethyl Ketone.

For data sheets and a sample, if desired, write to

SHELL CHEMICAL CORPORATION 100 Bush Street, San Francisco 6 · 500 Fifth Avenue, New York 18 Los Angeles · Houston · St. Louis · Chicago · Cleveland · Boston · Detroit

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