1928
DOI: 10.1002/jlac.19284600109
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Verhalten methoxylhaltiger Verbindungen gegen Aluminiumbromid

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Cited by 32 publications
(6 citation statements)
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“…Bromination of this stilbene derivative gave 1,2-di-o-tolyl-l ,2dibromoethane, mp 170-173°( lit.18 mp 171-172°). Dehydrobromination was effected using the same procedure as above with 19.05 g (0.052 mol) of this dibromide. The acetylene did not precipitate when the reaction mixture was poured into cold water.…”
Section: Resultsmentioning
confidence: 99%
“…Bromination of this stilbene derivative gave 1,2-di-o-tolyl-l ,2dibromoethane, mp 170-173°( lit.18 mp 171-172°). Dehydrobromination was effected using the same procedure as above with 19.05 g (0.052 mol) of this dibromide. The acetylene did not precipitate when the reaction mixture was poured into cold water.…”
Section: Resultsmentioning
confidence: 99%
“…205-207°. This cleavage gave results similar to those carried out with aluminum bromide. 19 The dihydroxybenzophenone was brominated directly in glacial acetic acid to give an 85% yield of 4,4'-dihydroxy-3,3',5,5'-tetrabromobenzophenone, m.p. 224-226°.20 A solution of 3.0 g. (0.0057 mole) of this ketone in 75 ml.…”
Section: Experimental Partmentioning
confidence: 99%
“…Both forward and reverse reactions are first order with respect to the organic reactant, since Eq. 2 holds (k, + k-,)t = 2.303 logic e/(ex) (2) where x and e are the fractions of organic material converted at the time, t, and at equilibrium, respectively, and ki and k-i are the specific reaction rate constants for the hydration and dehydration reactions, respectively. This is shown by the straight line character of the plot of logia (e -x) against time where the starting material is either mesityl oxide or diacetone alcohol (Fig.…”
mentioning
confidence: 99%