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- Draw a sawhorse projection for 3-aminobutan-2-ol representing where the two CH3-groups are syn-periplanar to each other.For each of the following compounds,determine whether each is optically active. For optically active compounds, identify the chiral carbon: ethane, 2-chloro-2-methylbutane, CH3CH(NH2)COOH, CH3CH2CHClCH3and CH3CH2CH2CH3. And for non-optical active compounds, just provide the structure of the compoundHow would you explain through tests that it is C5H12O and the other is CH3CH2CH2OH.
- i) Classify the molecule as being saturated or unsaturated. Give a reason for youranswer. ii) Classify the Carbon (marked with a *) as being 1o, 20, 30. State a reason foryour classification.The final four questions will require you to determine whether the compound in question will partition into the organic or aqueous phase. Which layer will phenylalanine partition into? Note: look up "zwitterions" water diethyl etherSuggest a reason why decane(CH3CH2CH2CH2CH2CH2CH2CH2CH2CH3) does not exhibitliquid crystalline behavior.
- How many constitutional isomers are possible for a triglyceride containing one molecule each of palmitic acid, oleic acid, and stearic acid? (b) Which of these constitutional isomers are chiral?Name all the functional groups of highly branched isoprenoids. Point out chiral centers and/or cis/trans double bonds if there are any and explain the significance of these structural components.What are all the steroisomers of this compound?