Exam 3: Stereoisomerism and Chirality

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What mass of (S)-(-)-mandelic acid is present in a 10 g sample which has an enantiomeric excess of 20% of the S-enantiomer?

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Which of the following structures is chiral? Which of the following structures is chiral?

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How much of the R enantiomer is present in 10 g of a mixture which has an enantiomeric excess of 20% of the S isomer?

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Which of the following substituents has the highest priority according to the Cahn-Ingold-Prelog system used in assigning R and S configurations?

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Which of the following is the definition of a pair of enantiomers?

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Which of the following is the definition of a meso compound?

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The specific rotation of the S-enantiomer of a compound is -120º. A student determines that a sample of the compound has a specific rotation of +60º. What mass of the S-enantiomer is present in 10 g of the sample

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How many chiral centers are there in the following molecule (the naturally occurring stereoisomer is camphor, a pungent moth repellent)? How many chiral centers are there in the following molecule (the naturally occurring stereoisomer is camphor, a pungent moth repellent)?

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The specific rotation of enantiomers have the same magnitude.

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Complete the following diagram so that it represents (S)-2-butanol. Complete the following diagram so that it represents (S)-2-butanol.

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Of the compounds listed below, only 2 has a chiral centers. Of the compounds listed below, only 2 has a chiral centers.

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An unknown sample is tested with a polarimeter for optical activity. The results of the test required no movement of the analyzer. This sample could be either a meso compound or a racemic mixture.

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How many isomers (constitutional and stereoisomers) exist for dimethylpentane?

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