Reagents

0.0(0)
Studied by 0 people
call kaiCall Kai
learnLearn
examPractice Test
spaced repetitionSpaced Repetition
heart puzzleMatch
flashcardsFlashcards
GameKnowt Play
Card Sorting

1/29

encourage image

There's no tags or description

Looks like no tags are added yet.

Last updated 6:45 PM on 4/25/26
Name
Mastery
Learn
Test
Matching
Spaced
Call with Kai

No analytics yet

Send a link to your students to track their progress

30 Terms

1
New cards
Bu4N+ F− (TBAF)
Silyl ether → alcohol (deprotection, reveals –OH)
2
New cards
H2, Pd/C
Alkene/alkyne → alkane (full hydrogenation)
3
New cards
Pyridine
No change; acts as base (used with acid chlorides, etc.)
4
New cards
CH2I2, Zn(Cu)
Alkene → cyclopropane (Simmons–Smith)
5
New cards
Hg(OAc)2, H2O / NaBH4
Alkene → Markovnikov alcohol (no rearrangements)
6
New cards
BH3, THF; H2O2, OH−
Alkene → anti-Markovnikov alcohol (syn addition)
7
New cards
ROOR, HBr
Alkene → anti-Markovnikov alkyl bromide (radical addition)
8
New cards
KF
No specific change; weak F− source
9
New cards
BH3, THF; H2O, OH−
Alkene → anti-Markovnikov alcohol (syn addition)
10
New cards
HX (HCl, HBr)
Alkene → Markovnikov alkyl halide (carbocation, rearrangements possible)
11
New cards
Br2 / Cl2
Alkene → vicinal dihalide (anti addition)
12
New cards
Br2, H2O
Alkene → halohydrin (OH on more substituted carbon)
13
New cards
OsO4 or KMnO4 (cold)
Alkene → syn diol (adds two OH)
14
New cards
O3, DMS or Zn
Alkene → aldehydes/ketones (ozonolysis cleavage)
15
New cards
O3, H2O2
Alkene → ketones/carboxylic acids (strong oxidation)
16
New cards
H2, Lindlar
Alkyne → cis-alkene (partial reduction)
17
New cards
Na, NH3 (liq)
Alkyne → trans-alkene (dissolving metal reduction)
18
New cards
HgSO4, H2SO4
Alkyne → ketone (Markovnikov hydration)
19
New cards
BH3 (bulky), H2O2, OH−
Terminal alkyne → aldehyde (anti-Markovnikov hydration)
20
New cards
PCC
1° alcohol → aldehyde; 2° alcohol → ketone (mild oxidation)
21
New cards
Na2Cr2O7, H2SO4
1° alcohol → carboxylic acid (strong oxidation)
22
New cards
TsCl, pyridine
Alcohol → tosylate (good leaving group)
23
New cards
SOCl2
Alcohol → alkyl chloride (inversion possible)
24
New cards
NaBH4
Aldehyde/ketone → alcohol (mild reduction)
25
New cards
LiAlH4
Ester/acid → alcohol (strong reduction)
26
New cards
RMgBr, then H3O+
Carbonyl → alcohol (C–C bond formation)
27
New cards
NaOH
Alkyl halide → alcohol (SN2 or E2)
28
New cards
NaOEt
Alkyl halide → alkene (strong base elimination)
29
New cards
NaCN
Alkyl halide → nitrile (adds carbon)
30
New cards
NH3
Alkyl halide → amine (substitution)