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Alcohols

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Total cards: 24•Content version: v3•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

have the general formula ROH, with the functional group -OH referred to as a hydroxyl group; named with suffix -ol, if not highest priority named as substituent with prefix hydroxy-

Back (Answer)

alcohol

#2
Front (Question)

benzene ring with hydroxyl groups; named for relative position of hydroxyl group: ortho- (adjacent carbons), meta- (one carbon in between), or para- (opposite sides of ring); more acidic than other alcohols because aromatic ring can delocalize the charge of the conjugate base

Back (Answer)

phenol

#3
Front (Question)

ability raises boiling and melting points of alcohols relative to corresponding alkanes, and increases solubility of alcohols

Back (Answer)

hydrogen bonding

#4
Front (Question)

groups that decrease acidity because they destabilize negative charges, such as alkyl groups

Back (Answer)

EDG (electron donating group)

#5
Front (Question)

groups that increase acidity because they stabilize negative charges, such as electronegative atoms and aromatic rings

Back (Answer)

EWG (electron withdrawing group)

#6
Front (Question)

only reagent that can oxidize primary alcohols only to aldehydes, would be oxidized to carboxylic acids by any stronger oxidizing agents

Back (Answer)

PCC (pyridinium chlorochromate)

#7
Front (Question)

oxidize primary alcohols to carboxylic acids and secondary alcohols to ketones

Back (Answer)

CrO3, Na2Cr2O7, or K2Cr2O7 ( chromium trioxide, sodium dichromate, or potassium dichromate)

#8
Front (Question)

can be oxidized to ketones by any common oxidizing agents

Back (Answer)

secondary alcohols

#9
Front (Question)

other forms alcohols can be converted to to make them better leaving groups for nucleophilic substitution reactions

Back (Answer)

mesylates and tosylates

#10
Front (Question)

contain functional group -SO3CH3, derived from methanesulfonic acid

Back (Answer)

mesylates

#11
Front (Question)

structure of a mesylate anion

Back (Answer)

Card back image
#12
Front (Question)

contain functional group -SO3C6H4CH3, derived from toluenesulfonic acid

Back (Answer)

tosylate

#13
Front (Question)

structure of a tosylate

Back (Answer)

Card back image
#14
Front (Question)

aldehydes and ketones can be protected by being converted to ____ and ____; formed by reacting two equivalents of an alcohol or a diol with a carbonyl

Back (Answer)

acetals and ketals

#15
Front (Question)

a primary carbon with two -OR groups and a H atom

Back (Answer)

acetal

#16
Front (Question)

a secondary carbon with two -OR groups

Back (Answer)

ketal

#17
Front (Question)

conversion of an acetal or ketal back to a carbonyl by catalytic acid

Back (Answer)

deprotection

#18
Front (Question)

what is happening in the reaction towards the right

Card front image
Back (Answer)

protection of a ketone by ketal formation using a dialcohol

#19
Front (Question)

synthesized through oxidation of phenols; resonance stabilized nucleophiles

Back (Answer)

quinones

#20
Front (Question)

vitamin K(1); biochemically relevant quinone important for photosynthesis and carboxylation of some clotting factors in the blood

Back (Answer)

phylloquinone

#21
Front (Question)

vitamin K(2); biochemically relevant quinone

Back (Answer)

menaquinone

#22
Front (Question)

a benzene ring with two hydroxyl groups

Back (Answer)

hydroquinone

#23
Front (Question)

contains two carbonyls and a variable number of hydroxyl groups produced by oxidation of quinones, adding a variable number of hydroxyl groups

Back (Answer)

hydroxyquinone

#24
Front (Question)

coenzyme Q; a biologically active quinone that acts as an electron acceptor in Complexes I, II, and III of the electron transport chain

Back (Answer)

ubiquinone