Ethylene may react with a halogen by a substitution reaction to give a vinyl halide and hydrogen halide, or the halogen may add to the double bond to give 1,2‐dihalo‐ethane or rearrange and give ethylidene halide. It is found that the symmetrical addition is favored in the case of each halogen. 1,2‐dihalo‐ethane, or the corresponding ethylidene compound may decompose to give ethylene and the halogen, or the vinyl halide and hydrogen halide. It is found that ethylene formation is favored in the bromine and iodine derivatives, whereas, in agreement with experiment, vinyl chloride and HCl would be produced from either 1,2‐dichlor‐ethane or ethylidene chloride. In most of the reactions considered mechanisms involving free radicals are slightly more probable than the corresponding unimolecular or bimolecular reactions.

1.
Sherman
and
Sun
,
J. Am. Chem. Soc.
56
,
1096
(
1934
).
2.
Sun
,
J. Chinese Chem. Soc.
41
,
98
(
1936
).
3.
See for example,
Van Vleck
and
Sherman
,
Rev. Mod. Phys.
7
,
167
(
1935
).
4.
For a more exact definition see
Eyring
,
J. Chem. Phys.
3
,
107
(
1934
).
5.
We shall illustrate the method by deriving the given relation in this particular case. Let the k’s be the specific reaction rate constants of the reactions concerned, and let E denote CH2 = CH2;EX, CH2CH2X; and K the equilibrium constant of reaction (1). Then, assuming that the rate of a reaction is proportional to the concentration of reacting substances, and the concentration of the free radicals do not change after the initial instant, we have
;
,
,
. Therefore 2k1(X2) = k1(X)2, or
,
,
. But, neglecting entropy, and remembering k = constant⋅e−A/RT,constant⋅e−A/RT = constant⋅e−A(2)/RT⋅e−ΔH/2RT = const⋅e−A(2)+12ΔH/RT or A = A(2)+12DX2.
6.
It is of course more probable that the monochlor‐ethylene free radical collide with the dichlor derivative than a chlorine atom, but the most likely chemical reaction would not be detectable in this case, i.e., CH2ClCH2Cl+CH2CH2ClCH2ClCH2+CH2ClCH2Cl.
7.
This value differs from the value given in reference 1 because in that paper ΔH7 of Table II was incorrectly calculated.
8.
This value differs from that given in reference 1 because there the same mechanism was assumed for the decomposition of the dichloride as for the other dihalide derivatives.
9.
F. O. Rice and O. K. Rice, Aliphatic Free Radicals (Johns Hopkins Press, 1935), pp. 70, 71, 184.
10.
L. S. Kassel, Kinetics of Homogeneous Gas Reactions (Chemical Catalog Company, 1932), p. 118.
11.
Cuthbertson
and
Kistiakowsky
,
J. Chem. Phys.
3
,
631
(
1935
).
12.
Stewart
and
Edlund
,
J. Am. Chem. Soc.
45
,
1014
(
1923
).
13.
Norrish
,
J. Chem. Soc.
123
,
3006
(
1923
).
14.
Davis
,
J. Am. Chem. Soc.
50
,
2769
(
1928
).
15.
G. Williams, J. Chem. Soc. 1747, 1758 (1932).
16.
D. M. Williams, ibid. 2911 (1932).
17.
Mitsukuri
,
Kinumaki
, and
Asaoda
,
J. Chem. Soc. Japan
54
,
1061
(
1933
).
18.
Bahr
and
Zieler
,
Zeits. f. Angew. Chem.
43
,
233
(
1930
).
19.
Stewart
and
Smith
,
J. Am. Chem. Soc.
51
,
3082
(
1929
).
20.
Kinumaki
,
J. Chem. Soc. Japan
54
,
142
(
1933
).
21.
Kharasch
,
McNab
, and
Mayo
,
J. Am. Chem. Soc.
55
,
2521
(
1933
).
22.
Kharasch
and
Hannum
,
J. Am. Chem. Soc.
56
,
712
(
1934
).
23.
Boeseken
and
Bastet
,
Rec. Trav. Chim.
32
,
187
(
1914
).
See also reference 9, p. 138,
and C. D. Hurd, Pyrolysis of Carbon Compounds (Chemical Catalog Company, 1929), p. 131.
24.
Arnold
and
Kistiakowsky
,
J. Chem. Phys.
1
,
166
(
1933
).
25.
Ogg
,
J. Am. Chem. Soc.
58
,
607
(
1936
).
26.
See C. D. Hurd, reference 23, p. 131.
27.
Reference 23.
28.
For an evaluation of this constant see
Eyring
,
J. Chem. Phys.
3
,
107
(
1935
). It is also possible that the rate determining step for a reaction involving a proton, may involve a leakage through a potential energy barrier.
29.
See, for example, reference 3.
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