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look for H in DIFF environments
identical H’s count as 1 signal

look for O-CH3 on sheet
n + 1 rule:
0 - 1 - singlet
1 - 2 - doublet
2 - 3 - triplet
3 - 4 - quartet
Bonds:
C - 4
N - 3
O - 2
H - 1

inside the benzene ring only 2 diff signals

most upfield = lowest ppm

rmr to count BOTH neighboring atoms
so if one is a singlet and the other is a doublet it would be a doublet

start w/ DOU
name
use n + 1 backwards
use splittting to eliminate options

major = endo = UNDER bridge
stereochem stays the same ALWAYS ONLY for alkenes
Always 6 membered ring will be product
Diene = 4 pi bonds C = C - C = C
Dienophile = C = C OR C=- C triple bond
Diene + alkene (1 double bond) = 1 double bond
Diene + alkyne (1 triple bond) = 2 double bonds

conjugated:
C = C - C = C
1 single bond between
isolated:
C = C - C - C = C
2+ single bonds between
Cumulated:
C = C = C
double bonds touch

first step: number all the carbons in the conjugated diene
low temp: 1,2 addition
high temp: 1,4 addition DOUBLE BOND MOVES to middle
is it mark, or anti mark?
mark: HCl HBR HI, H2O, H+, Hg(OA)2 MORE substituted carbon
If MINOR: do the opposite addition

SO3 + H2SO4 = -SO3H
Br2 + FeBr3 = -Br
Cl2 + FeCl3 = -Cl

Only when X is attached to a carbon w/ ONLY SINGLE BONDS
R - Cl + AlCl3 = -R
R - Br + AlBr3 = -R
R - COCl + AlCl3 = -COR
Since this quesiton has a DB it would be D) No Reaction