Chapter 12: Q 12 P (page 385)
Question: Where might the following compound have IR absorptions?
Short Answer
Absorption bands seen at 2210-2260 , 1690 and 1640-1680 .
Chapter 12: Q 12 P (page 385)
Question: Where might the following compound have IR absorptions?
Absorption bands seen at 2210-2260 , 1690 and 1640-1680 .
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Get started for freePhenol,, is a stronger acid than methanol, , even though both contain an OH bond. Draw the structures of the anions resulting from loss of from phenol and methanol, and use resonance structures to explain the difference in acidity.
Predict the products for the reactions in Problem 8-26 if each were run in DMSO with water. Show the complete mechanism including appropriate regiochemistry and stereochemistry.
The infrared spectrum of the compound with the mass spectrum shown below has strong absorbances at 1584, 1478, and 1446 cm-1 . Propose a
structure consistent with the data.
The following carboxylic acid can't be prepared from an alkyl halide by either the nitrile hydrolysis route or the Grignard carboxylation route.Explain.
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