Science Homework Help
Organic Chemistry Fingerprint and Diagnostic Signals Question
I’m studying for my Chemistry class and don’t understand how to answer this. Can you help me study?
1. Deduce the identity of compound A and B, whose IR spectrum shows the following fingerprint and diagnostic signals.
Compound A
- 3500-2600 (broad) cm-1
- 1710 (intense) cm-1
- 1200 ( medium) cm-1
Compound B
- 3400-3200 (broad) cm-1
- 3100-2900 (broad) cm-1
- 1200 ( medium) cm-1
A.
Compound B is an alcohol
Compound A is a carboxylic acid
B.
Compound B is an alcohol
Compound A is an aldehyde
C.
Compound B is an aldehyde
Compound A is an carboxylic acid
D.
Compound A is an aldehyde
Compound B is an carboxylic acid
E.
Compound A is an alcohol
Compound B is a carboxylic acid
2. Deduce the identity of compound A and B, whose IR spectrum shows the following important fingerprint and diagnostic signals.
Compound A
- 3100-3080 ( medium, sharp) cm-1
- 3000-2850 (strong, intense) cm-1
- 1610 (medium, sharp) cm-1
Compound B
- 3300-3250 ( strong, sharp) cm-1
- 3000-2850 (strong, intense) cm-1
- 2100 (medium, sharp) cm-1
A.
Compound A is an Alkene ( sp2 C-H present)
Compound B is an Alkyne ( sp C-H present)
B.
Compound B is an Alkene ( sp2 C-H present)
Compound A is an Alkyne ( sp C-H present)
C.
Compound A is an Alkene ( sp2 C-H absent)
compound B is an Alkene ( sp2 C-H present)
D.
Compound B is an Alkene ( sp2 C-H absent)
compound A is an Alkene ( sp2 C-H present)
E.
Compound A is an Alkane
compound B is an Alkene
3. Which compounds would be consistent with the IR and NMR spectrum given below. (REFER TO LAB 2 PDF ATTACHED).
- Draw the structure of the compound
- Match all the peaks/ signals on the IR ; H-NMR and C-NMR spectra with the functional groups/ protons/ carbons present in the predicted molecule.
Chemical Formula: C6H12O; Molecular Weight: 100.16