Identify each of the following structures as chiral or achiral. If chiral, indicate the chiral carbon. OH a. CH3-CH-CH3 Br b. C. Br CH3-CH-CH d. OH CH3-CH2-C-CH3 CH3 CI CI CH3-C-CH2-CH-CH3 CH3 e OH OH I
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- CHE 132 Ch. 18 - Carbohydrates 1. Classify the following carbohydrates in terms of the carbonyl type and the number of carbon atoms. a) Ctz-cH-CH-CH-ビーH CH--C2 OH oH OH OH OH ribose dehyinoxyacetone <) H-ċ-CH-CH-CH2 enythrese 2. Identify the chiral centers in the following molecules. HC-CH-CH2 ーC-CH OH OH OH gluperaldehyde dahydroxyacetone C) CH-CH-CH-CH- OH OH OH ーC-H ribose 3. Draw Fischer projections of the following carbohydrates. (do -for moleculed in #2)Optical Isomers Optical isomers have a chiral carbon atom. A chiral (or asymmetric) carbon atom is one that has four different groups attached to it. a H This carbon is chiral because it has four different groups attached to it. H,N CH, OH C - Identify which carbon (number) has the chiral center CI OH CH3 H H. H2N H- C-H H C F HICI H2. Indicate whether each of the following molecules are chiral or achiral. Circle the chiral carbon(s) if present in each structure. CH3 H–C–CH,CH CH₂CH₂CH₂ a. H CH3 b. C. OH
- Indicate whether each of the following molecules are chiral or achiral. Circle the chiral carbon(s) if present in the structure. CH 3 H. C=C%3DC%3D0 H3C BICH 2 C CH2CH 3 CH3 H. b. С. a.1. In the structure provided choose the option YES or NO to indicate if the carbon atoms are chiral. H 2. Assign the absolute configuration of the asymmetric/chiral centers in the provided structures a, b and c. a. a. C-H HO-CH3 H b. NH₂ 3. For the following two structures compared in parts A and B, determine whether they are enantiomers OR diastereomers OR the same structure drawn differently (non-bonding electrons not included for clarity). d. Br Br OH door OH Br b. CH3 HC OH H-C O Br $R= C. OH Br Br OH Br 1Which carbon atom (a - e) in the molecule shown below corresponds to a stereocentre (chiral carbon)? H3C H H.C. a О O a e C b c d H3C CH3 CH3
- H ÇI CH3-C-COOH он CH3-C-CH2Br 1. ČI a b 81. Consider the structures above. Which of these two contains a stereocenter? Draw thestructure on your answer sheet and mark the stereocenter with an asterisk. 82. Which of these two is a chiral molecule? Explain your answer. 83. Which of these two can exist as a pair of enantiomers? 84. Draw the pair of enantiomers using three-dimensional representation.Identify which of the compound is chiral.a. T-butyl alcoholb. 2,2-dimethylpropanec. 1,2,4,5-tetramethylcyclohexaned. 2-hydroxypropanoic acid5. Assign R and S to each chiral center. Br H. CI NH2 H, OH H... OCH3 CH3 H. NC A A [ [ Choose ] [ Choose ] [ Choose ] C [ [ Choose ] D
- 16.SR-10: Identify, interpret, and draw representations of isomers and conformers. This includes chiral and achiral structures. 1. Draw the following compounds in their bond-line structures as indicated by the Newman projection. Use solid wedges or dashed wedges to denote the correct arrangement at any chiral center (chiral carbon). OH b. OH a. H₂ H H₂C H₂C CH₂OH2. Draw the optical isomers of CH3-CHOH-CHOH-CH3 . INDICATE the absolute configuration of each chiral center. Which are enantiomers? Which are diastereomers? Is there any meso compound present? Identify if yes.. Determine whether each structure is chiral. CI a. HC-CH, b. CH3-CH-CH-CH3 ČI Cl CH3 c. CH3-CH2-OH CI d. HC-CH2 CH; Br