“…252, 308 (1889). After chlorination or bromination of high-molecular, straightchain hydrocarbons with, for example, N-chloro-or Nbromosuccinimide, t-butyl hypochlorite or hypobromite [I] the isomeric chlorides of n-heptane, n-octane, n-decane and the isomeric bromides of n-heptane and n-octane were The changes in the concentration of DPNH with time were followed by spectrophotometry [l], and the catalytic activity was calculated in units per ml [2]. The reaction mixture comprised 3 mi of 0.05 M triethanolamine buffer (pH 8.0), 0.045 ml of 0.01 M DPNH, 0.03 ml of 0.26 M EDTA, 0.1 ml of 3 M ammonium acetate, and 0.03 ml of 10-7 M GIDH.…”