8. One stereoregular form of polystyrene (A) has a 'H NMR spectrum containing a triplet centered at about 1.4 ppm and a quintet at about 1.9 ppm. Another stereoregular form (B) has an octet at about 1.6 ppm and a quintet at about 2.3 ppm. (Both spectra also exhibit phenyl proton resonances further downfield.) Interpret the spectra and determine which corresponds to isotactic and which to syndiotactic. (Syndiotactic polystyrene was first reported by N. Ishihara and co-workers in a 1986 paper. You may wish to locate the paper and check your answer.)

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8. One stereoregular form of polystyrene (A) has a 'H NMR
spectrum containing a triplet centered at about 1.4 ppm and a
quintet at about 1.9 ppm. Another stereoregular form (B) has an
octet at about 1.6 ppm and a quintet at about 2.3 ppm. (Both
spectra also exhibit phenyl proton resonances further
downfield.) Interpret the spectra and determine which
corresponds to isotactic and which to syndiotactic. (Syndiotactic
polystyrene was first reported by N. Ishihara and co-workers in
a 1986 paper. You may wish to locate the paper and check your
answer.)
Transcribed Image Text:8. One stereoregular form of polystyrene (A) has a 'H NMR spectrum containing a triplet centered at about 1.4 ppm and a quintet at about 1.9 ppm. Another stereoregular form (B) has an octet at about 1.6 ppm and a quintet at about 2.3 ppm. (Both spectra also exhibit phenyl proton resonances further downfield.) Interpret the spectra and determine which corresponds to isotactic and which to syndiotactic. (Syndiotactic polystyrene was first reported by N. Ishihara and co-workers in a 1986 paper. You may wish to locate the paper and check your answer.)
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