he compound given is 3,3-dimethyl-2-butanone.
Interpret the 1H-NMR spectrum, detailing chemical shifts and splittings, draw the structure of the compound and label hydrogens (a,b,c,d,e) for the signals. amk UIT IKLUUENCY PPM INTENSITY 1071.875 575.350 572.946 2.1432 1.1505 1.1475 IHNMR 6.882 16.205 16.467 CRJI :- (HVEPSE PAJDE Expansion of precious H UMR PARTIN, CHINYERIE PACEE 7/12/90 Scanned with CamScanner Apu
Interpret the 13C-NMR spectrum and draw the structure of the compound and label carbons (a,b,c,d,e) for the signals.
13C NMR - CANECH I NVENTE PROCE 7/12/9 ZW 77 PW O AD has AQ 1031 La 1.000 11/CH 919.090 PPW/CH24 sn 2915897 impunity Solut Sc
Interpret the IR spectrum and draw the structure of the compound, and label functional groups that are responsible for the stretches.
%Transmittance 4000 3500 3000 2968.54 2908.33 2873.23 Wavenumbers (cm-1) 2500 2000 1704.83 1500 1476.98 1464.86 1429.23 1394.
amk UIT IKLUUENCY PPM INTENSITY 1071.875 575.350 572.946 2.1432 1.1505 1.1475 IHNMR 6.882 16.205 16.467 CRJI :- (HVEPSE PAJDE. 7/12/90 : Scanned with CamScanner EL To y
Expansion of precious 'H UMR PARTIN, CHINYERIE PACEE 7/12/90 Scanned with CamScanner Apu
13C NMR - CANECH I NVENTE PROCE 7/12/9 ZW 77 PW O AD has AQ 1031 La 1.000 11/CH 919.090 PPW/CH24 sn 2915897 impunity Solut Scanned with CamScanner Talec
%Transmittance 4000 3500 3000 2968.54 2908.33 2873.23 Wavenumbers (cm-1) 2500 2000 1704.83 1500 1476.98 1464.86 1429.23 1394. 13 1364.88 1354.05 1274.31 1224.09 1134.51 1000 953.48 832.86 Scanned with CamScanner