Search results
Results from the WOW.Com Content Network
HOCH 2 (CH 2) 2 COOH 2-oxobutanoic acid: α-ketobutyric acid: CH 3 CH 2 COCOOH 3-oxobutanoic acid: acetoacetic acid diacetic acid: CH 3 COCH 2 COOH 4-oxobutanoic acid: succinic semialdehyde: OHC(CH 2) 2 COOH butanedioic acid: succinic acid: HOOC(CH 2) 2 COOH 2-methylpropanedioic acid: methylmalonic acid: HOOCCH(CH 3)COOH -butenedioic acid ...
When necessary, the position of the hydroxyl group is indicated by a number between the alkane name and the -ol: propan-1-ol for CH 3 CH 2 CH 2 OH, propan-2-ol for CH 3 CH(OH)CH 3. If a higher priority group is present (such as an aldehyde , ketone , or carboxylic acid ), then the prefix hydroxy- is used, [ 19 ] e.g., as in 1-hydroxy-2 ...
The hydrogen centre in the carboxyl group (−COOH) in carboxylic acids such as acetic acid can separate from the molecule by ionization: CH 3 COOH ⇌ CH 3 CO − 2 + H + Because of this release of the proton (H +), acetic acid has acidic character. Acetic acid is a weak monoprotic acid. In aqueous solution, it has a pK a value of 4.76. [21]
CH 3 (CH 2) 4 COOH: Goat fat 7: Enanthic acid: Heptanoic acid: CH 3 (CH 2) 5 COOH: Fragrance 8: Caprylic acid: Octanoic acid: CH 3 (CH 2) 6 COOH: Coconuts: 9: Pelargonic acid: Nonanoic acid: CH 3 (CH 2) 7 COOH: Pelargonium plant 10: Capric acid: Decanoic acid: CH 3 (CH 2) 8 COOH: Coconut and Palm kernel oil: 11: Undecylic acid: Undecanoic acid ...
The acetate anion, [CH 3 COO] −,(or [C 2 H 3 O 2] −) is one of the carboxylate family. It is the conjugate base of acetic acid. Above a pH of 5.5, acetic acid converts to acetate: [1] CH 3 COOH ⇌ CH 3 COO − + H + Many acetate salts are ionic, indicated by their tendency to dissolve well in water.
Reduction in carbon emissions across the United States and especially in Ohio exist because of natural gas. Due to changes in electricity generation, older coal-fired generation plants with large ...
In solution, it can ionize by a loss of a proton to produce the lactate ion CH 3 CH(OH)CO − 2. Compared to acetic acid, its pK a is 1 unit less, meaning lactic acid is ten times more acidic than acetic acid. This higher acidity is the consequence of the intramolecular hydrogen bonding between the α-hydroxyl and the carboxylate group.
The state Oil and Gas Commission has sided with the Department of Natural Resources in a case involving who should pay for a $1.3 million environmental cleanup caused by a leak from an Ohio ...