15E.6 Flashcards

1
Q

how does the 13C NMR spectrum look like for a compound

A

it is usually a straight horizontal line just above the horizontal axis but with vertical lines called signals or peeks that show the signals produced by 13C

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2
Q

the number of vertical line in a 13C NMR spectrum tells you

A

the number of different chemical environments of carbon atoms in the molecule, but not necessarily the total number of carbon atoms

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3
Q

the potion of the vertical lines on the x axis in an 13C NMR tells you

A

the chemical shift of each carbon atom, and with reference to the list of chemical shifts, it will allow you to deduce the chemical environment

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4
Q

a carbon atoms chemical environment is based on

A

the groups it is attached to for example CH3 - CH2 - CH2 - OH the CH3 and the CH2s are attached to different groups so they would have different chemical environments so we would except them to have different peek in the 13C NMR

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5
Q

how many peaks should propan-2-ol have

A

its structure CH3 - CH(OH) - CH3 it would have two peaks since the CH3s have the same chemicals environment

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6
Q

why would the peak of CH3s be more than the peak of CH(OH) in CH3 - CH(OH) - CH3

A

because the CH3s would have the same signal so the peak is caused by 2 carbons instead of one

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7
Q

analysis of the Propan-1-ol NMR spectrum

A

page 145

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8
Q

analysis of the Propan-2-ol NMR spectrum

A

page 145

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