C" NMR Peaks Aldehydes RCOR Aldehydes and ketones Carbarylic R(CO)X Carborylc acid derivatives Ntrile Nitrile RCN Akyne Akyne RCCR RCH20 RCH20 RAC PAC RICH RICH RCH2X X- C-C, CHO, Br, CIN ACHZX R2CH2 RECH2 RCH3 RCH3 TMS TMS 220 200 180 160 140 120 100 80 40 20 Typical chemical shits in 13C-NMR 9) Why do the peaks of associated with aldehydes (both in H NMR and C" NMR) appear so much further downfield than other peaks? c" NMR Peaks 8.
C" NMR Peaks Aldehydes RCOR Aldehydes and ketones Carbarylic R(CO)X Carborylc acid derivatives Ntrile Nitrile RCN Akyne Akyne RCCR RCH20 RCH20 RAC PAC RICH RICH RCH2X X- C-C, CHO, Br, CIN ACHZX R2CH2 RECH2 RCH3 RCH3 TMS TMS 220 200 180 160 140 120 100 80 40 20 Typical chemical shits in 13C-NMR 9) Why do the peaks of associated with aldehydes (both in H NMR and C" NMR) appear so much further downfield than other peaks? c" NMR Peaks 8.
Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Calibri (Bo.. v 11
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Sensitivity
C13 NMR Peaks
Aldehydes
RCO)R
Aldehydes and ketones
Carbaxylic
R(CO)X
Carbaxylic acid derivatives
Ntrile
Nitrile RCN
CC
C-C
Alkyne
Akyne R-CC-R
RCH20
RCH2-O
R4C
RAC
R3CH
R3CH
RCH2X
X= C-C, C-O, Br, CI, N
RCH2X
R2CH2
RECH2
RCH3
RCH3
TMS
TMS
220
200
180
160
140
120
100
80
60
40
20
Typical chemical shifts in 13c-NMR
9) Why do the peaks of associated with aldehydes (both in H NMR and C NMR) appear so much further
downfield than other peaks?
C13 NMR Peaks E
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E English (United States)
O Focus
295 words
白"
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Calibri (Bo.. v 11
v A A
E vE v E v E E
Aa v
AaBbCcDdEe
AaBbCcD AaBbCcDdE AaBb
AaBbCcDdEe
BIU V ab
A • I v A v
Paste
х, х
E= ==
No Spacing
Normal
Heading 1
Heading 2
Title
Styles
Pane
Dictate
Sensitivity
C13 NMR Peaks
Aldehydes
RCO)R
Aldehydes and ketones
Carbaxylic
R(CO)X
Carbaxylic acid derivatives
Ntrile
Nitrile RCN
CC
C-C
Alkyne
Akyne R-CC-R
RCH20
RCH2-O
R4C
RAC
R3CH
R3CH
RCH2X
X= C-C, C-O, Br, CI, N
RCH2X
R2CH2
RECH2
RCH3
RCH3
TMS
TMS
220
200
180
160
140
120
100
80
60
40
20
Typical chemical shifts in 13c-NMR
9) Why do the peaks of associated with aldehydes (both in H NMR and C NMR) appear so much further
downfield than other peaks?
C13 NMR Peaks E
Page 5 of 5
E English (United States)
O Focus
295 words
白
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