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Hydoboration Oxidation has what kind of addition?
Syn Addition
Adding X2 an Alkene has what kind of addition?
Anti Addition
H2 and Lindlard's Catalyst
Turns alkyne to a Cis alkene- "Sisters lie"
H2 and Pt-C
Turns an alkyne to an alkane- "Poof!"
Li/NH3 and Na/ND3
Turns an alkyne to a trans alkene
BH3/AcOH
turns an alkyne to a cis alkene
LAH and NaBH4
Used as hydride reducing agents H has a negative charge and attacks, then a proton is delivered to form H2O or an alcohol (Markovinkov alcohol) *Used to open epoxide rings to form alcohols
LAD
Strong Base- usually attacks a hydrogen
DMSO
the oxygen is usually used to attack a hydrogen
SOCl2 and PCl3 come with
pyridine
POCl3 is used to make
an alkene from an alcohol- dehydration of an alcohol (without rearrangement)
SOCl2 and PCl3
conversion of alcohols to alkyl chlorides or bromides
Addition of HX to an alkene results in
syn and anti addition to make an alkane with H and X
Addition of water and H2SO4 to an alkene results in
syn and anti addition to make an alkane(alcohol) with H and OH
X2 and H20 to an alkene results in
an alkane with X and OH added in anti addition
Hydroboration oxidation of Internal Alkenes results in
Ketone (C=0 with a C on the other C)
Hydroboration oxidation of Terminal Alkenes results in
Aldehyde (C=O with an H on the other C)
NBS and NCS
Souce of Br2 and Cl2
CHCL3 + KOH
turns double bond into a triangle with two chlorines coming off of it
CH2I2 + Zn + Hg
turns double bond into a triangle
tert-butyl group
Carbon with three methyl groups
sec-butyl group
carbon with a methyl group, ethyl group and H
ethylene group
CH2=CH2
isopropyl
Carbon with two methyl groups and a H
methylene group
$=CH2
vinyl group
CH2=CH$
allyl group
CH2=CCH2$
phenyl group
R-Benzene ring
sp3 C on NMR
chemical shift ~0.9-2ppm
z=C-C-H on NMR
chemical shift ~1.5-2.5ppm
CtriplebondC on NMR
~2.5 ppm
sp3 C-Z on NMR
~2.5-4 ppm
C=C on NMR
4.5-6 ppm
Benzene ring on NMR
6.5-8 ppm
C=O on NMR
9-10 ppm
OH-C=O on NMR
10-12 ppm
RO-H or R-N-H on NMR
1-5 ppm

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