Question 18 1 points Consider an El mechanism for the reaction of bromocyclopentane with hydroxide as...
Consider an El mechanism for the reaction of bromocyclopentane with hydroxide as shown below. Which elementary step or sequence of steps from the list below would outline the step(s) for an El mechanism? Η. Η Η ΕΙ + OH ***BE Η. Η Η Η. Η (1) H "Br + Br Η. Η Η H (2) Η CUBI Θ + Br ΝΗ, Η Η HO (3) IBI + HO + Br Η. Η Η HO Θ CBI + HO + Br"...
Consideran i mechanism for the reaction of bromocyclopentane with hydroxide as shown below. Which elementary step or sequence of steps from the list below would outline the step(s) for an El mechanism? Н. HH E1 + OH Η. Η Η H H (1) + B HHH Η. Η -Н (2) ПВ + Br H. H H HO: (3) (В HOB Η. Η H HO Н. н H HO (3) . iB + H,0 + Br н Н H НО (4)...
unsure why this is wrong where I put my arrows. please explain Consider the El reaction of the tertiary halide shown. H Н. .Н OH H :Br: Br: NaOH H product Step 1: Add curved arrow(s). Step 2: Add curved arrow(s). Select More Erase Draw Rings More Erase Select Draw Rings C Br H C н Br re Ts e13
Choose a mechanism of the following hydrolysis reaction. (Practice the Skill 19.23ad) Practice the Skill 19.23ad Choose a mechanism of the following hydrolysis reaction. он H30+ HO OH HH H .H . . 10 HH :د* :: : :5 ..: OH | HH 01 H H مقامی شیکه - فان من H 0 م ..: OH TH 10! Hн -H co- Н HOH .::. : H H .. HT , 10 پڑا ہے مكان .. | من :o H 0...
11. Show the mechanism for an El reaction below. Number your carbons in each step!!! (15 pts) Hint: regenerate HCl in the last step! H-0 o C H-CI (catalyst) te ga na af. non - Hot OH (solvent)
Jame: . Complete this mechanism for the following substitution reaction. Note: this reaction is balanced. H-Br Н,0 OH -CH3 H20 Step 1: proton transfer Step 2: lose water Step 3: attack the carbocation Br -CH3 . Each reaction above is reversible. In question 1, what effect would adding more HBr have on the equilibrium? Would there be more or less alkyl bromide product present at equilibrium? . Two dehydrations can occur on glycerol, the principle carrier molecule in vaping devices....
"ОН Step 1 Fill in the following reaction scheme based on the Roman numerals provided below: но Η Ν. HO HOH НО-Н Step 2 H-OH H-OH H ОН HO -Η HO -H НО. H HOH HO -H HO+H CH, OH CH OH CH OH Step 3 HCN cat. HCI H,0 HIO NH,OH NaBHA EROH - 11 III IV V NaOCH, Bra H.0 VII cat HCI CH,OH но" Pa/Baso Hy XI VI VIII х HNO H.O heat XI H,02 Fox(50) XII...
Question 17 Predict the major product(s) for the reaction shown below. (choose all correct answers) Br2 ?? Br Br Br Br Br Br Br பி Question 18 Which of the reaction steps, shown below, would be part of the mechanism for the acid-catalyzed hydration of trans-but-2-ene? (choose all correct answers) OH но н-о-s-он + H нн H-O-S-OH Он + о H H онн нн :Он он H H нн O нн H-O-S-OH он + OH o=S-O
please show all steps including each mechanism (arrows) and also if SN1 has any rearrangements of carbocation intermediate through a hydride shift and/or methyl shift. DO NOT NEED ELIMINATION. ONLY SUBSTITUTION. Sy1/E1 versus S2/E2 Learning Checks Draw the major organic substitution and/or elimination products in the following reactions. If no reaction is possible, write “No Reaction". Substitution Product(s) Elimination Product(s) 2) 2) OH BrCH K* -Ot-Bu NaOCH н"Сн, сн,он нсн, Ph NaOCH Br H CH3OH CH NaOCH NaOH T.CH, I...
Consider the following reaction mechanism: 1) Initiation Br2 → 2 Br• 2) Propagation (here a cycle of two steps) Br• + H2 → HBr + H• H• + Br2 → HBr + Br• 3) Termination 2 Br• → Br2 This reaction is catalyzed by platinum. Wat causes the bromine to split in the initiation step? Does the platinum influences this or is it just due the weak bonding between Br-Br?