2. For the SN2 reaction depicted below, (a) please form all possible products and (b) draw...
2. For the SN2 reaction depicted below, (a) please form all possible products and (b) draw the mechanism using curved arrow notation that explains the formation of these products. (5 pts) Br H e.. K:OCH2CH3 CH3 THF
2. For the S2 reaction depicted below, (a) please form all possible products and (b) draw the mechanism using curved arrow notation that explains the formation of these products. (5 pts) Br,H CH3 KOCH,CH THF
2. For the Su2 reaction depicted below, (a) please form all possible products and (b) draw the mechanism using curved arrow notation that explains the formation of these products. (5 pts) Br OO. к :осн,сH, CH3 THF
2. For the Sw2 reaction depicted below, (a) please form all possible products and (b) draw the mechanism using curved arrow notation that explains the formation of these products. (5 pts) Br. H . сна KOCH2CH3 THE
Quiz 3 (20 pts) October 30, 2019 CHEM 2401 1. For the following substitution reaction, please (a) calculate the AH endothermic process? (5 pts) . (b) is this reaction an exothermico Сн, H-C-Br сн. & H-OH . H-C-OH сн. H-Br CH3 Bond dissociation energies (CH3)2CH-Br 285 kJ/mol (CH3)2CH-OH 401 kJ/mol H-OH 498 kJ/mol H-Br 368 kJ/mol 2. For the Sn2 reaction depicted below, (a) please form all possible products and (b) draw the mechanism using curved arrow notation that explains...
Question 1 Consider the reaction of the compound shown below with the labeled O* (in bold). (4 points) -Ситн ? CH2CH3 NaOH H20 CH3 a) Draw a detailed mechanism showing this hydrolysis reaction and show which of the products will contain the labeled O*. For full marks, make sure to include curved arrow notation to illustrate bond formation/cleavage in a step-by-step manner.
PLEASE ANSWER ALL QUESTIONS Question 5 The reaction below occurs via SN2 and E2 reaction mechanisms. The question only requires you to address the E2 reaction only. For the E2 reaction: Use Newman projections to show the relationship between the leaving group and the beta-hydrogen on the carbon labeled with the asterisk ("). 1. If the leaving group and the beta-hydrogen on the carbon labeled with the asterisk (1) are not in the correct orientation, show the result of the...
Complete the multistep mechanism for the formation of each of the possible monochlorination products from reaction of 2,2,4,4-tetramethylpentane with chlorine in light. Map Complete the multistep mechanism for the formation of each of the possible monochlorination products from reaction of 2,2,4,4-tetramethylpentane with chlorine in light. Initiation step in the presence of light. Use curved arrows to show the mechanism of the propagation steps below. (Click on the blue box to toggle through four possible arrow choices.) a) Formation of the...
Below is the SN1 reaction of (S)-2-iodopentane and bromide (Br–). Complete the mechanism by providing the missing curved arrow notation, lone pairs of electrons, and nonzero formal charges. Be sure to draw the two organic products that will be produced in the third box. Below is the SN1 reaction of (S)-2-iodopentane and bromide (Br). Complete the mechanism by providing the missing curved arrow notation, lone pairs of electrons, and nonzero formal charges. Be sure to draw the two organic products...
2. Draw a detailed, stepwise mechanism to show how the products of this reaction form. Clearly draw the structures of all reactive intermediates. Use curved arrows and include all formal charges. Hint: both Sy1 and SN2 chemistry is required. (2 pts) Oor 21Oo..mo