. Explain why do you choose that product and mechanism or in case something else happens explain why. CH3 KOCH )a H3C- CH3 Solvent: Ethanol HCI c-O4 Solvent: Ethanol CH, коссн H,C- -CH3 Solvent: Toluene HCI CH3 но CH3 Solvent: Toluene H3C CH, KOCCH 33 .CI Solvent: Toluene -CH3 CH,
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- Below is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- Rate = k [CH3CH2Br][CH3COO-] Which mechanism would best fit the data?For SN1 Explain the order in which 1o (primary) alkyl halides reacted (fastest to slowest) and explain why. The 1o primary alkyl halides are: (see picture below) 1-chlorobutane 1-bromobutane 1-chloro-2butene benzylchloridePlease provide the intermediates, steps, and labels. Thanks!
- Show the steps of the next reaction in detail. And explain why it's hard to go along with the dotted line.Alkyl diazonium salts (shown below) are considered "super" leaving groups; a consequence of this is that they tend to be contact explosives What quailities make alkyl diazonium salts such excellent leaving groups?Chemistry please provide the flow of electrons aswell!! thank you! using the starting material (on the left) to determine the sythetic route which will be the most reaosnable and effective to theres none, you have to start witth the begin products to get to finish needed by using the minmium reagents and reactions needed to get to the final product
- Please help with the following ochem mechanisms.... 1. Provide the stepwise mechanisms for the following reactions (see attached picture)Which reactions will proceed faster in a polar, aprotic solvent? (CH3)2CHCH2I+Na+N3−(CH3)2CHCH2I+Na+N3− (CH3)3CBr+HSCH2CH3(CH3)3CBr+HSCH2CH3 CH3CH2CH2Br+Na+CN−CH3CH2CH2Br+Na+CN− (CH3)2CHOSO2CH3+HOCH(CH3)2Please give me the final product following reaction . Feel free to write out each step! thatd be greatly appreciated!
- 2. In not more than three (3) sentences, explain why terminal alkynes are acidic.3. What impurities are removed when acetylene gas is made to pass through an acidifiedsolution of CuSO4?4. Explain the difference in the rate of free radical bromination reactions of toluene and cyclohexane.please answer part two (Please answer "What is BP of the solvent, and the authors state... why is that important"). thank you "The 3-Sulfolene is the prime molecule used for synthesis for the 1,3-butadiene molecule. The mechanism involves breaking of two C-S bonds in 3-sulfolene to generate 1,3-butadiene in the presence of heat. The reaction can be shown as below: This reaction is a type of pericyclic reaction that involves breaking and making of bonds in a single step and hence there will be no intermediate formed. The solvent used here is water." https://www.bartleby.com/questions-and-answers/3-sulfolene-a-butadiene-source-for-a-diels-alde-synthesis.-please-be-prepared-to-take-a-quiz-on-this/8bf8358d-dbdf-46f9-97db-6f744d66c0cdWhy we need step 3 before step 4? a. Because the nitro group increases the electrophilicity at the ortho positions which is where the bromine is added. b. Because the amine group is a strong ortho, para director which is what controls the regiochemical outcome of this bromination. c. Step 4 is unessesary. The symmetry of compound 3 allows for the bromination to be regioselective and give compound 5. 5. There will be a mixture of products because there is no selectivity for a major product.