given: tables of ir, 1h, and 13c absorptions allowed

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Given: Tables of IR, 1H, and 13C absorptions Allowed: Calculator Approx. IR absorptions Class Group Wavenumber (cm^-1) Alkane C–H 2850-1960 Alkene C–H 3020-3100 C=C 1640-1680 Alkyne C–H 3300-3320 C≡C 2100-2260 Alcohol O–H 3400-3650 C–O 1050-1200 Ether C–O 1070-1150 Aldehyde C=O 1670-1780 Ketone Ester Carboxylic acid

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Page 1: Given: Tables of IR, 1H, and 13C absorptions Allowed

Given: Tables of IR, 1H, and 13C absorptions

Allowed: Calculator

Approx. IR absorptions

Class Group Wavenumber (cm^-1)

Alkane C–H 2850-1960

Alkene C–H 3020-3100

C=C 1640-1680

Alkyne C–H 3300-3320

C≡C 2100-2260

Alcohol O–H 3400-3650

C–O 1050-1200

Ether C–O 1070-1150

Aldehyde C=O 1670-1780

Ketone

Ester

Carboxylic acid

Page 2: Given: Tables of IR, 1H, and 13C absorptions Allowed

Spectroscopy (~20%)

Page 3: Given: Tables of IR, 1H, and 13C absorptions Allowed

14.57 Label the indicated IR peak with the proper functional groups of its compound

14.58 Label the indicated IR peaks with the proper functional groups of its compound

Page 4: Given: Tables of IR, 1H, and 13C absorptions Allowed
Page 5: Given: Tables of IR, 1H, and 13C absorptions Allowed
Page 6: Given: Tables of IR, 1H, and 13C absorptions Allowed
Page 7: Given: Tables of IR, 1H, and 13C absorptions Allowed

Synthesis (~20%)

Page 8: Given: Tables of IR, 1H, and 13C absorptions Allowed
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Page 10: Given: Tables of IR, 1H, and 13C absorptions Allowed

(Create own problems: changing position of double bond; halide)

Page 11: Given: Tables of IR, 1H, and 13C absorptions Allowed

Mechanisms (~13%)

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Structures (~13%)

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Isomers (~13%)

Page 17: Given: Tables of IR, 1H, and 13C absorptions Allowed

________omers have identical chemical and physical properties,

while ________omers have different properties.

Page 18: Given: Tables of IR, 1H, and 13C absorptions Allowed

Reactivity (~13%)

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Nomenclature (~7%)

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