of 23 Macmillan Learning Draw the substitution product formed in the reaction. CH3 H3C C-C Br H₂ CH3 I H₂O Draw the product. Select Draw Templates More / # C H O Br 3 C Erase
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A: see the attatchmentExplanation:Step 1: Step 2: Step 3: Step 4:
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- Identify the organic functional group(s) of the reactant, the reaction type, and predict the functional group(s) of the product(s) then draw the major product(s) The reactant is:a. deoxytetroseb. alcohol pentosec. ketohexosed. aldotriosee. aldopentoseThe reaction type is:a. acetal formationb. oxidation (benedict's)c. hemiacetal formationd. acetal hydrolysise. reduction (hydrogenation)f. mutarotationThe product should be:a. alpha 1-4 disaccharideb. deoxyhexosec. carboxylic acid pentosed. alcohol pentosee. alpha pyranosef. no reactionI. True or False ____________7] Salivary amylase can be use to hydrolyze 1,4 glycosidic bonds of cellulose.____________8] Lobry de Bruyn-van Ekenstein Transformation take place when a sugar is treated with a strongly basic reagent.The rate constant for the uncatalyzed reaction of two molecules of glycine ethyl ester to form glycylglycine ethyl ester is 0.6 M- 1s - 1. In the presence of Co2 +, the rate constant is 1.5 * 106 M- 1s - 1. What rate enhancement does the catalyst provide?
- An oligosaccharide isolated from an organism is found tocontain two glucose residues and one galactose residue.Exhaustive methylation followed by hydrolysis producedtwo glucoses with methoxy groups at positions 2, 3,and 6 and galactose with methoxy groups at positions2, 3, 4, and 6. What is the structure of the originaloligosaccharide?The enzyme that catalyzes the Ca ¬ Cb bond cleavage reaction that converts serine to glycine removes thesubstituent (R) bonded to the a-carbon in the first step of the reaction. Starting with PLP bound to serine inan imine linkage, propose a mechanism for this reaction. (Hint: The first step involves removal of the protonfrom serine’s OH group.)A hydrocarbon of unknown structure has the formula C8H10. On catalytic hydrogenation over the Lindlar catalyst, 1 equivalent of Η2 is absorbed. On hydrogenation overa palladium catalyst, 3 equivalents of Η2 are absorbed. (a) How many degrees of unsaturation are present in the unknown structure? (b) How many triple bonds are Present? (c) How many double bonds are present? (d) How many rings are present? (e) Draw a structure that fits the data.