the last row of the table. Circle the regioisomeric product that has numbers of each category of proton that match those observed in the NMR spectrum of carvone epoxide.

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Chapter1: Chemical Foundations
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In order to determine (or to confirm the 13C NMR analysis of) the regioselectivity of the addition, determine the
number of signals that would appear in each region of the spectrum for the carvone starting material and the two
regioisomeric products. For instance, each product has two methyl carbons, so you should write "2" in each cell in
the last row of the table. Circle the regioisomeric product that has numbers of each category of proton that match
those observed in the NMR spectrum of carvone epoxide.
CH3
CH3
CH3
Н.
H
H.
H
H.
CH3
CH3
CH3
H.
Н-С-C (4.5-6.8 ppm)
Н-С-О (3.4-4.2 ppm)
sp³ CH (1.8-3.0 ppm)
sp³ CH3 (1.0-1.8 ppm)
Transcribed Image Text:In order to determine (or to confirm the 13C NMR analysis of) the regioselectivity of the addition, determine the number of signals that would appear in each region of the spectrum for the carvone starting material and the two regioisomeric products. For instance, each product has two methyl carbons, so you should write "2" in each cell in the last row of the table. Circle the regioisomeric product that has numbers of each category of proton that match those observed in the NMR spectrum of carvone epoxide. CH3 CH3 CH3 Н. H H. H H. CH3 CH3 CH3 H. Н-С-C (4.5-6.8 ppm) Н-С-О (3.4-4.2 ppm) sp³ CH (1.8-3.0 ppm) sp³ CH3 (1.0-1.8 ppm)
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