Quarterly Journal of the Chemical Society of London, Volume 1 |
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Page 94
... Acetic Acid By P. G. Blake * and G. E. Jackson , Chemistry Department , University College , Cardiff CF1 3NR The homogeneous thermal decomposition of acetic acid has been studied between 530 and 762 ° in a flow system . Below 600 ...
... Acetic Acid By P. G. Blake * and G. E. Jackson , Chemistry Department , University College , Cardiff CF1 3NR The homogeneous thermal decomposition of acetic acid has been studied between 530 and 762 ° in a flow system . Below 600 ...
Page 137
... Acetic Pivalic Ether Acetonitrile 1000 % 1170 820 Benzoic 610 Acetic 64 88 p - NO , CH , CO , N ( CH , Ph ) , ... Acetic P - CH , CÔ , CH , NO , P.P ' - NO2 CH1 · ČO2 · С ̧H ̧ · NO2 Acetic 130 No catalysis the sensitivity of the various ...
... Acetic Pivalic Ether Acetonitrile 1000 % 1170 820 Benzoic 610 Acetic 64 88 p - NO , CH , CO , N ( CH , Ph ) , ... Acetic P - CH , CÔ , CH , NO , P.P ' - NO2 CH1 · ČO2 · С ̧H ̧ · NO2 Acetic 130 No catalysis the sensitivity of the various ...
Page 430
... acetic anhydride and acetic acid , pyridine being used as catalyst . The product , m.p. 161-162 ° ( lit. , 3 159 ° ) had a 1H n.m.r. spectrum which showed signals at 7.58 ( s , CH , CO ) and 2.0—3 · 3 ( m , Ar - CH ) . 5 - Acetoxy - 2,4 ...
... acetic anhydride and acetic acid , pyridine being used as catalyst . The product , m.p. 161-162 ° ( lit. , 3 159 ° ) had a 1H n.m.r. spectrum which showed signals at 7.58 ( s , CH , CO ) and 2.0—3 · 3 ( m , Ar - CH ) . 5 - Acetoxy - 2,4 ...
Contents
Physical organic chemistry | 1 |
Aromatic reactivity Part XXXVIII Protodesilylation of 12dihydrobenzocyclobutene indan and tetralin | 12 |
Aromatic reactivity Part XL Additional substituent effects in protodetrimethylsilylation | 21 |
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absorption acetic acid activation added addition alcohol Amer analysis angles appears aqueous atom base benzene bond bromide calculated carbon carbon tetrachloride Chem chemical chloride compared complex compounds concentration conformation constants containing corresponding coupling derived described determined DISCUSSION effect electron energy equation esters ethanol ether expected experimental experiments factor Figure followed formation formed further gave give given hydrogen hydrolysis increase indicate initial intermediate involving kinetic less measured mechanism method methyl mixing mixture mole molecular molecule nitration observed obtained occurs organic oxidation oxygen peaks peroxide Phys plot position possible prepared present pressure proton radical rate constants ratio reaction reactivity reduced relative reported requires resonance respectively ring salts shifts showed shown similar sodium solution solvent spectra spectrum structure studied substituent suggested Table temperature values yield