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A: Given compounds:
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- Indicate wether the following pairs of compounds are constitutional isomers, diastereomers, enantiomers, or the same compoundFor each pair of structures shown, indicate hether the two species are constitutional isomers, enantiomers, diastereomers of one another, or identical moleculesidentify asymmetirc centers with the symbol (*)
- 9) Which of the following terms best describes the following pair of molecules? A) Geometricisomers B) Configurational isomers C) Constitutional isomers D) Conformational isomerWhich has the greater polarizability? Explain.(a) Br⁻ or I⁻ (b) CH₂=CH₂ or CH₃—CH₃(c) H₂O or H₂Secis-1,2-Dimethylcyclohexane is optically inactive even though it has two chirality centers. Explain.
- Classify the folowing pair of molecules as enantimoers or diastereomersndicate the relationship betwwen each of the following pairs of moelcules as: a) identical; b) constitutional isomers; c) enantiomers; d) diastereomers; or e) not even isomesrs; etc. Give the reason of your choice.Which of the following can exist as enantiomers?
- Classify the following structures as E/Z-isomers:the molecule in questionrepresents an enantiomer or ameso compound? This molecule isoptically active? Justify, including inits definition the concept of compoundmeso and enantiomer.Most naturally occurring amino acids have chiral centers (the asymmetric a carbon atoms)that are named (S) by the Cahn–Ingold–Prelog convention (Section 5-3). The commonnaturally occurring form of cysteine has a chiral center that is named (R), however.(a) What is the relationship between (R)-cysteine and (S)-alanine? Do they have the oppositethree-dimensional configuration (as the names might suggest) or the same configuration?(b) (S)-Alanine is an l-amino acid (Figure 24-2). Is (R)-cysteine a d-amino acid or anl-amino acid?