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for carboxylic acids
drop -e add -oic acid
for acyl haldies
drop -e add -oyl halide
for esters
alkyl and drop -e add -oate
for amides
drop -e and add -amide and use N-alkyl groups
for carboxylic acids on rings
if single, add carboxylic acid and don’t drop -e
for acyl halides on ring
add -carbonyl halide
for esters as ring
if single, add carboxate
for amides on ring
if single, carboxamide
esters in full cylic version
lactone
amines in full cyclic versions
lactam
esters, acids, amide and carboxylic acids are
h20 soluble
acyl halide reacts with h20 so
solubility not relevant
those with carbonyl & h bonds have
high bp
those with carbonyl and no h bond have
low bp
high bp example
amides
low bp example
ketone
acid halides in nature
don’t exist, react violently with water
esters in nature
in fruit flavor, beeswax, and fats
example of esters
jasmine, banana and apple
carboxylic acid in nature
fatty acids
example of carboxylic acids
rancid butter, vinegar, ants, and wet goat
amides in nature
dna, proteins
example of amides
caffeine