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- Give the IUPAC name each of the following polymers? 1 HO(CH,CH,CH, NH(CH,)-NH-) -H 3-(-(C₂Hs)-CHCH-Ph-) 2-(-O-Ph-) 3- (-CH,CHO (COCH))),| Exercises 317 9.21 Identify the reactants from which the following molecules were prepared. If an acetal, identify the carbonyl compound and the alcohol; if an imine, identify the carbonyl compound and the amine; if an alcohol, identify the carbonyl compound and the Grignard reagent (red = 0, blue = N): (a) (b) (c)Explain this ? "Organic synthesis is the systematic preparation of a compound from areadily available starting material by one or many steps".
- Iees] Use the References to access important values if needed for this question. Draw the organic product that is expected to form when the following compound is oxidized under biological conditions. oxidation CH3CH2SH reduction • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • If no reaction occurs, draw the organic starting material. cP opy aste Previc ChemDoodleProvide the product of the reaction in the given image.[5] Write the structure of the product of the reaction of (S)-3-bromo-3-methylhexane with ethanol (CH,CH,OH).
- ences] Use the References to access important values if needed for this question. Draw the organic product that is expected to form when the following compound is oxidized under biological conditions. oxidation CH,CH,SH reduction • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • If no reaction occurs, draw the organic starting material. C. opy aate Pre ChemDoodle"Draw the structure of the expected organic product formed in the following reactions including correct stereochemistry. If the product is racemic indicate this by either drawing both isomers or drawing one and writing racemic. Assume all reagent are present in excess unless otherwise noted. If no reaction occurs, state "No Reaction".3. Predict the products of the following reactions, Draw out the condensed structural formulas for the reactants and the products. Name the products (organic compounds only.) d) Halogenation of 3-methyl-1-butyne with Cl2 (1:2 ratio) ensard-S-araldah- (o e) Hydration of 1,3-dimethylcylobutene f) Alkylation of benzene with 2-chlorobutane