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carboxylic acids
these are organic compounds that have a carboxylic group attached to an alkyl group (RCOOH) or to any aryl group (ArCOOH)
carboxylic acids
these can be mono carboxylated, multi carboxylated, substituted, or they maybe aromatic
true
t/f: one of the general methods of preparign carboxylic acids is by the oxidation of primary alcohols or aldehydes
KMnO4
this is an oxidizing agent that helps in the preparation of carboxylic acids
primary alcohols
these are oxidized first into an aldehyde before turning into a carboxylic acid
true
t/f: reactions like carboxylic acid creation is a common thing in biological systems done by enzymes like alcohol and aldehyde dehydrogenase found in the liver.
aldehyde dehydrogenase
this is found in the liver and is used to break down ingested alcohols in the liver to form a less harmful form called acetate
formic acid, acetic acid, and lactic acid
these are the only acids that are liquids at room temperature
true
t/f: low molecular weight carboxylic acids are soluble in water and therefore, lie under class S1
true
t/f: water insoluble acids dissolve in both sodium hydroxide solution and sodium bicarbonate solution, being classified under class A1 and when they react with sodium bicarbonate, they evolve carbon dioxide gas
proton
the acidic properties of carboxylic acids are attributed to the (blank) of the carboxyl group
mono carboxylic acids
these are weak acids except formic acid which is the strongest
true
t/f: the tendency of the alkyl group to release electrons weakens the acid; thus formic acid is the strongest.
true
t/f: on the other hand, presence of electron withdrawing groups (such as halogens) especially on the alpha carbon increases the acidity
true
t/f: reactions of carboxylic acids are related to the proton as in salt formation reactions
true
t/f: Removal of the hydroxyl group as in conversion to derivatives such as esters, amides, or acid chlorides