Chapter 28: Problem 84
Enantiomers always (a) have an asymmetric carbon; (b) have different physical properties; (c) change the color of light; (d) rotate polarized light; (e) none of these.
Chapter 28: Problem 84
Enantiomers always (a) have an asymmetric carbon; (b) have different physical properties; (c) change the color of light; (d) rotate polarized light; (e) none of these.
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Get started for freeThe following terms are all related to stereoisomers and their optical activity. Explain the meaning of each: (a) dextrorotatory; (b) levorotatory; (c) racemic mixture; (d) \((R)\).
Describe what is meant by each of the following terms, using specific examples where appropriate: (a) polypeptide; (b) protein; (c) N-terminal amino acid; (d) \(\alpha\) helix; (e) denaturation.
If one strand of a DNA molecule has the base sequence TCT, what must be the sequence on the opposite strand? Draw a structure of this portion of the double helix, showing all hydrogen bonds.
The so-called Ruff degradation is a chain-shortening reaction in which an aldose chain is shortened by one C atom, hexoses, for example, being converted into pentoses. In the Ruff degradation, the calcium salt of an aldonic acid (the corresponding carboxylic acid of an aldose) is oxidized with hydrogen peroxide. Ferric ion catalyzes the reaction. The calcium salt of the aldonic acid necessary for the Ruff degradation is obtained by oxidizing an aldose with an aqueous solution of bromine and then adding calcium hydroxide. The reaction scheme is as follows where \(R\) represents the rest of the chain of the aldose. (a) Show that D-glucose can be degraded into D-arabinose. Which other aldose can be degraded into D-arabinose? (b) Which two monosaccharides can be degraded into D-glyceraldehyde by employing the Ruff degradation only once?
Write the formulas of the species expected if the amino acid phenylalanine is maintained in (a) \(1.0 \mathrm{M}\) HCl; (b) \(1.0 \mathrm{M} \mathrm{NaOH} ;\) (c) a buffer solution with \(\mathrm{pH}=5.7\).
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