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Ochem CH 17 exam 3
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name this group
\
c=o
/
carbonyl group
name this group
R
l
C=O
l
H
aldehyde
name this group
R
l
C=O
l
R
ketone
order of precedence in numbering:
______>_________>_____
carbonyl > alcohol > alkene/alkyne
C=O > OH > C=C C
=
C
aldehydes have (-??) endings
ketones have (-???) endings
aldehydes have
(-al)
endings
ketones have
(-one)
endings
order of precedence in numbering:
aldehydes ( ___ ) ketones
aldehydes
>
ketones
an aldehyde with a ketone as a substituent has what in its name?
"OXO"
ex
: 5-oxohexanal
CH
3
C(O)CH
2
CH
2
CH
2
C(O)H
an aldehyde attached to a ring structure has what ending?
carbaldehyde
ex: cyclopentanecarbaldehyde
name this substituent
O
ll
CCH
3
acetyl
in a cyclic molecule, carbonyl always gets #___ and substituents always get _____ possible number
in a cyclic molecule, carbonyl always gets
#1
and substituents always get
lowest
possible number
Common name & IUPAC name
Common name : formaldehyde
IUPAC name: methanal
Common name & IUPAC name
Common name: acetone
IUPAC: propanone
Common name & IUPAC name
Common name: acetaldehyde
IUPAC: ethanal
Common name & IUPAC name
Common name: acetophenone
IUPAC name: 1-phenylethanone
Common name
diethyl ketone
Common name
methyl ethyl ketone
Oxidation of alcohol:
2
o
alcohol--(_____)->ketone
2
o
alcohol--CrO
3
->ketone
Oxidation of alcohol:
1
o
alcohol--(_____)->aldehyde
1
o
alcohol--PCC->aldehyde
F-C acylation:
Ozonolysis of Alkenes
Hydration of Alkynes
Aldehydes are _____ reactive than ketones
MORE ; due to sterics & carbonyl polarization
Electronegative substituents ________ reactivity of C=O
INCREASE ; by intensifying + charge on C which allows greater reactivity with Nucleophiles
Carbonyl & Nucleophilic Addition:
If good Nucleophile =>
If good Nucleophile = Nuc adds to C first, then O is protonated
Carbonyl & Nucleophilic Addition:
If weak Nucleophile=>
If weak Nucleophile = O protonates first, then Nuc adds to C
"hemiacetal" has ...
"hemiacetal" has OH,OR on same C
"acetal" has ...
"acetal" has OR,OR on same C
a "thiol" is ...
a "thiol" is like an alcohol with S instead of O
ex: R-OH => R-SH
The 3 steps for using Protecting Groups:
1) Protect carbonyl using ethylene glycol
2) Undergo SN2 rxn
3) Deprotect carbonyl with water and H
+
What is this compound and what is it used for?
HO-CH
2
-CH
2
-OH
ethylene glycol ; used as a Protecting Group to limit reactivity of carbonyls
Name NH
3
ammonia
CH
3
NH
2
is a ____ amine
primary
(CH
3
)
2
NH is a ____ amine
secondary
(CH
3
)
3
N is a ____ amine
tertiary
Primary amine = ?
Primary amine = "imine"
The 2 steps for adding an amine to a carbonyl are . . .
1) Addition of amine to C (N-C) causing e
-
in C=O d.b. to move to O as LPE and H+ to shift to O-
2) Elimination of 1 eq H
2
O
What is the net change when adding a primary amine to a carbonyl?
R'
l
C=O + NH
2
R ----> ?
l
H
Replace O by N and lose 2 H's from N
R'
l
C=NR
l
H
Name H
2
N-NH
2
hydrazine
Name
\
C=N-NH
2
/
hydrazone
Secondary amine = ?
Secondary amine = "enamine"
A Deoxygenation Reaction does what?
replaces C=O with CH
2
Deoxygentation via Wolff Kishner Reduction is accomplished by adding what in 2 steps?
Author
ffloyd
ID
72093
Card Set
Ochem CH 17 exam 3
Description
flashcards for CH 17 ochem exam 3
Updated
2011-03-10T22:01:31Z
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