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Interpretation:
The products formed on oxidation of each of the given compounds with periodic acid are to be predicted.
Concept Introduction:
Vicinal
Reaction of a vicinal diol with periodic acid results in the cleavage of bonds that connect the two hydroxyl groups to the adjacent carbon atoms in the diol molecule.
Depending on the number of hydrogen atoms attached to these carbon atoms,
If the hydroxyl group is attached to a primary carbon atom, formaldehyde is produced at that carbon atom.
If the hydroxyl group is attached to a secondary carbon atom, aldehyde is produced at that carbon atom.
If the hydroxyl group is attached to a tertiary carbon atom, a ketone is produced at that carbon atom.
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Chapter 16 Solutions
ORGANIC CHEMISTRY (LL)-W/SOLN.>CUSTOM<
- Nonearrow_forwardTransmitance 3. Which one of the following compounds corresponds to this IR spectrum? Point out the absorption band(s) that helped you decide. OH H3C OH H₂C CH3 H3C CH3 H3C INFRARED SPECTRUM 0.8- 0.6 0.4- 0.2 3000 2000 1000 Wavenumber (cm-1) 4. Consider this compound: H3C On the structure above, label the different types of H's as A, B, C, etc. In table form, list the labeled signals, and for each one state the number of hydrogens, their shifts, and the splitting you would observe for these hydrogens in the ¹H NMR spectrum. Label # of hydrogens splitting Shift (2)arrow_forwardNonearrow_forward
- Draw the Lewis structure of C2H4Oarrow_forwarda) 5. Circle all acidic (and anticoplanar to the Leaving group) protons in the following molecules, Solve these elimination reactions, and identify the major and minor products where appropriate: 20 points + NaOCH3 Br (2 productarrow_forwardNonearrow_forward
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