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- Will the dicarboyl or ketone react faster. Draw a picture to explain ur answerWhich of the following compounds will test positive with Tollen’s Test? 1 answer only.Using the choices below (image) answer the following questions: 1. Reaction of Butanal with R-Mg-X 2. Reaction of Acetone with PropylMgCl 3. Substitution of reaction between ROH and SOCl2 4. Reduction of aldehydes 5. Dehydration of alcohols No need to futher explain the answers
- Draw the following a) N-methylpropanamideb) cis-2-heptenec) 2-hexanone d) butylbutanoatee) 3-chloropentanoic acid f) 2,2-dibromo-butanalg) 2-octanolh) 1-propynei) butylethylmethylamine j) butylpropyletherWhich of the following statements is false? A. None B. All C. Positive result for a ketone is indicated by a red-orange precipitate using chromic acid test. D. Positive result for an aldehyde is indicated by a greenish precipitate using 2,4-DNPH reagent. E. Positive result for an aldehyde is indicated by an orange to red precipitate using Tollen’s reagent.identify the error in each name. Then correct the name. a. 2-pentanal b. N,N-diethyl-N-methylpentanamide
- (1) what reagent is used to convert p-amino phenol to quinone (2) Draw two different kekule's structures for pyrene and under line the more stableWrite the expected product for each of the following reaction: 2-Butanone + NaCN, HCl -------------> ? Acetone + 2 eq. CH3CH2OH, H+ -----------> ? Benzaldehyde + 1 eq. benzyl alcohol, H+ ---------> ?a. Draw a three-dimensional structure for the following steroid. b. What is the structure of the single stereoisomer formed by reduction of this ketone wrth H2, Pd-C? Explain why only one stereoisomer is formed.
- 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 reactionPropose a strategy for the given synthesis. The answer is not GA or GAK.Glutamic acid is synthesized by the following reaction sequence. Draw a stepwise mechanism for Steps [1]–[3].