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- Alkynes undergo many of the same reactions that alkenes do. What organic product(s) would you expect when the following compound is treated with 2 equiv H2, Pd/C?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 x 106 M-1s-1. What rate enhancement does the catalyst provide?so we know that fischer esterification is a type of organic reaction that involves the formation of an ester from a carboxylic acid and an alcohol in the presence of an acid catalyst. am I correct to assume that a fisher esterification mechanism would look different than the above nucleophilic addition reaction? If they are different you you present the Fisher esterification mechanism of the reaction of acetic acid with pentanol in the presence of an acid catalyst, sulfuric acid and explain the mechanism
- I have this task in organic chemistry (book: Brown's introduction to organic chemisty, global edition). Task 10:42. In (a) I have to tell what the funcion of K2CO3 is in step 1. Is it that CO32- take the hydrogen atom in 1-napthol? Will it then be a SN2 mechanism? In (b) I have to name the amine used in step 2 to form Propanolol. But I can't really find out how to come up with an amine that will make that reaction. Here are two pictures of the task:Identify the organic functional group of the product, the reaction type, and predict the functional group of the reactant. Then choose the most likely reactant from the reaction below.The product is a(n)a. aldehydeb. aromaticc. alcohold. alkanee. alkeneThe reaction type is :a. oxidationb. hydrationc. reduction (hydrogenation)d. hydrolysise. dehydrationThe reactant should be a(n)a. ketoneb. alkenec. alkaned. alcohole. esterThe most likely reactant is molecule :a. Bb. Ac. Dd. CFor the answers I got alcohol, hydrolysis, alkene, and C. But I got one of them wrong. What are the correct answers?Identify the organic functional group of the product, the reaction type, and predict the functional group of the reactant. Then choose the most likely reactant from the reaction below.The product is a(n)a. aldehydeb. aromaticc. alcohold. alkanee. alkeneThe reaction type is :a. oxidationb. hydrationc. reduction (hydrogenation)d. hydrolysise. dehydrationThe reactant should be a(n)a. ketoneb. alkenec. alkaned. alcohole. esterThe most likely reactant is molecule :a. Bb. Ac. Dd. C
- Fill in the following missing organic structures. Consider stereochemistry (R/S and/or E/Z –cis/trans) and possible carbocation rearrangements.Identify the organic functional group of the product, the reaction type, and predict the functional group of the reactant. Then choose the most likely reactant from the reaction below.The product is a(n)a. aromaticb. alkenec. aldehyded. alcohole. etherThe reaction type is :a. dehydrationb. oxidationc. reduction (hydrogenation)d. hydratione. hydrolysisThe reactant should be a(n)a. aldehydeb. alkenec. esterd. alkynee. alcoholThe most likely reactant is molecule :a. Both C and D would form the productb. D onlyc. Bd. C onlye. ADoes the data provide evidence for the claim that the reaction of Br2 with alkenes proceeds via anti‐addition? The mleting point of the product was found to be 234.5-235.5C chemical reaction: trans-stilbene+pyrimindine tribromide --->acetic acid 1,2-di bromo-1,2-diphenylethane product was trans-1,2-dibromo-1,2-diphenylethane
- hw synthesize foll. products start acetylene CH=CH and organic inorganic reagentsIn cells, vitamin C exists largely as its conjugate base X. X is anantioxidant because radicals formed in oxidation processes abstract thelabeled H atom, forming a new radical that halts oxidation. Draw thestructure of the radical formed by H abstraction, and explain why this Hatom is most easily removed.Does the data provide evidence for the claim that the reaction of Br2 with alkenes proceeds via anti‐addition? The mleting point of the product was found to be 234.5-235.5C chemical reaction: trans-stilbene+pyrimindine tribromide --->acetic acid 1,2-di bromo-1,2-diphenylethane