Back to marketplace

Aldehydes and Ketones I: Electrophilicity and Oxidation-Reduction

No description yet. This curated deck is ready for daily study.

Total cards: 13•Content version: v3•Public deck•Updated: 8/1/2026

Card preview (13)

#1
Front (Question)

carbonyl characteristic dictated by polarity of double bond; carbon has a partial positive charge making it electrophilic

Back (Answer)

reactivity of carbonyl

#2
Front (Question)

water adds to a carbonyl, forming a geminal diol

Back (Answer)

hydration reaction

#3
Front (Question)

hydration reaction

Back (Answer)

Card back image
#4
Front (Question)

formed when one equivalent of alcohol reacts with an aldehyde/ketone, via nucleophilic addition

Back (Answer)

hemiacetal/hemiketal

#5
Front (Question)

hemiacetal/hemiketal formation

Back (Answer)

Card back image
#6
Front (Question)

formed when two equivalents of alcohol react with an aldehyde/ketone, via nucleophilic substitution

Back (Answer)

acetal/ketal

#7
Front (Question)

acetal/ketal formation

Back (Answer)

Card back image
#8
Front (Question)

can form when nitrogen and nitrogen derivatives react with carbonyls

Back (Answer)

imines

#9
Front (Question)

imine formation

Back (Answer)

Card back image
#10
Front (Question)

can form when hydrogen cyanide reacts with carbonyls

Back (Answer)

cyanohydrins

#11
Front (Question)

cyanohydrin formation

Back (Answer)

Card back image
#12
Front (Question)

_____ (aldehydes and/or ketones) can be oxidized by KMNO4, CrO3, Ag2O, or H2O2

Back (Answer)

aldehydes

#13
Front (Question)

____ (aldehydes and/or ketones) can be reduced by LiAlH4 or NaBH4

Back (Answer)

aldehydes and ketones