Ethyl 2-hydroxy cyclohexanecarboxylate

C9H16O3 cis-2-hydroxy-cyclohexanecarboxylic acid ethyl ester 6149-52-6... 

HMnOi - + MnOi" + OH accounts for the major reaction pathway. In the reaction with hydroxy-cyclohexanecarboxylic acids,a complex pH dependence is observed, the mechanism involving complex formation between the neutral hydroxy-acid and the permanganate. The intermediate complex is, however, considered to undergo a (reversible) deprotonation prior to the rate-determining electron transfer step. Acid-dependent and -independent paths have also been described in the oxidation of ethyl acetate in perchloric acid. The mechanism of the fast reaction between Mn " and nitrite has been investigated in glycine and phthalic acid buffers. The rate law may be expressed as... 

Benzoic acid ethyl ester. See Ethyl benzoate Benzoic acid, 4-(((ethylphenylamino) methylene) amino)-, ethyl ester. See N-(p-Ethoxycarbony I phenyl )-N -ethy l-N -phenylformamidine Benzoic acid, hexahydro-. See Cyclohexanecarboxylic acid Benzoic acid, hexyl ester. See Hexyl benzoate Benzoic acid, 4-hydroxy- Benzoic acid, p-hydroxy-. See 4-Hydroxybenzoic acid Benzoic acid, 2-hydroxy-, butyl ester. See Butyl salicylate... 

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