Questions from Organic Chemistry


Q: Identify the reagents you would use to convert oleic acid into each

Identify the reagents you would use to convert oleic acid into each of the following compounds: a. Stearic acid b. Ethyl stearate c. 1-Octadecanol d. Nonanedioic acid e. 2-Bromostearic acid

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Q: Limonene is an optically active compound isolated from the peels of lemons

Limonene is an optically active compound isolated from the peels of lemons and oranges. a. Is limonene a monoterpene or a diterpene? b. Treatment of limonene with excess HBr yields a compound with t...

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Q: Starting with the following compound and using any other reagents of your

Starting with the following compound and using any other reagents of your choice, outline a synthesis for trimyristin:

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Q: Acrolein is an α,β-unsaturated aldehyde that is used

Acrolein is an α,β-unsaturated aldehyde that is used in the production of a variety of polymers. Acrolein can be prepared by treating glycerol with an acid catalyst. Propose...

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Q: The following compound was isolated from nerve cells: /

The following compound was isolated from nerve cells: a. Describe how this compound differs in structure from fats and oils. b. Three products are obtained when this compound is hydrolyzed with aque...

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Q: The amidomalonate synthesis can be used to prepare amino acids from alkyl

The amidomalonate synthesis can be used to prepare amino acids from alkyl halides. When the amidomalonate synthesis is used to make glycine, no alkyl halide is required. Explain.

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Q: Predict the major product(s) in each of the following

Predict the major product(s) in each of the following cases:

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Q: Show how racemic valine can be prepared by each of the following

Show how racemic valine can be prepared by each of the following methods: a. The Hell–Volhard–Zelinsky reaction b. The amidomalonate synthesis c. The Strecker synthesis

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Q: How many different pentapeptides can be constructed from the 20 naturally occurring

How many different pentapeptides can be constructed from the 20 naturally occurring amino acids in Table 25.1? From Table 25.1:

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Q: Using an asymmetric catalytic hydrogenation, identify the starting alkene that you

Using an asymmetric catalytic hydrogenation, identify the starting alkene that you would use to make L-histidine.

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