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4-Aminophenol (or para-aminophenol or p-aminophenol) is an organic compound with the formula H 2 NC 6 H 4 OH. Typically available as a white powder, [ 3 ] it is commonly used as a developer for black-and-white film , marketed under the name Rodinal .
Substance Formula 0 °C 10 °C 20 °C 30 °C 40 °C 50 °C 60 °C 70 °C 80 °C 90 °C 100 °C Barium acetate: Ba(C 2 H 3 O 2) 2: 58.8: 62: 72: 75: 78.5: 77: 75
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
Heat capacity, c p [2] 96 J/(mol K) Liquid properties Std enthalpy change of formation, Δ f H o liquid: −249.4 kJ/mol Standard molar entropy, S o liquid: 200.4 J/(mol K) Enthalpy of combustion, Δ c H o –1785.7 kJ/mol Heat capacity, c p: 125.5 J/(mol K) Gas properties Std enthalpy change of formation, Δ f H o gas: −218.5 kJ/mol Standard ...
In the presence of suitable catalysts, two acetone molecules also combine to form the compound diacetone alcohol (CH 3)C=O(CH 2)C(OH)(CH 3) 2, which on dehydration gives mesityl oxide (CH 3)C=O(CH)=C(CH 3) 2. This product can further combine with another acetone molecule, with loss of another molecule of water, yielding phorone and other ...
The molecular formula C 6 H 7 NO (molar mass: 109.13 g/mol) may refer to: Aminophenols. 2-Aminophenol; 3-Aminophenol; 4-Aminophenol; Nicotinyl alcohol ...
Because acetic anhydride is not stable in water, the conversion is conducted under anhydrous conditions. To a decreasing extent, acetic anhydride is also prepared by the reaction of ketene with acetic acid at 45–55 °C and low pressure (0.05–0.2 bar). [8] H 2 C=C=O + CH 3 COOH → (CH 3 CO) 2 O (ΔH = −63 kJ/mol)
Isophorone is produced on a multi-thousand ton scale by the aldol condensation of acetone using KOH. Diacetone alcohol, mesityl oxide, and 3-hydroxy-3,5,5-trimethylcyclohexan-1-one are intermediates. A side product is beta-isophorone, where the C=C group is not conjugated with the ketone. [4]