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.
My question is what does the platinum do? I know that platinum is able to split the H2 bond but is that the only function of the platinum in this reaction?
Consider the following reaction mechanism: 1) Initiation Br2 → 2 Br• 2) Propagation (here a cycle...
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?
Q3: Determine the rate of formation of HBr considering the mechanism of chain reaction: Initiation: Br2 -R1→2Br Propagation: H-+ Br2-3→ HBr + Br. -K, Br2 Termination: 2Br
Instructions: draw in the mechanism for each reaction Initiation Propagation Termination HBr H202 Br
Predict the major product of the following reaction, and draw complete mechanisms for the initiation and propagation steps. Propose 2 termination steps. Label each elementary step. Br2 hv Initiation: Propagation: Predict the major product of the following reaction, and draw complete mechanisms for the initiation and propagation steps. Propose 2 termination steps. Label each elementary step. Br2 hv Initiation: Propagation:
please answer these questions Given the following complex reaction mechanism for the reaction H2(g) + Br2(g) → 2 HBr (g): Br2 → 2 Brº (rate constant ka) Br + H2 → HBr +H* (rate constant kb) Hø + Br2 → HBr + Br" (rate constant ke) H + HBr → H2 + Brº (rate constant kd) Br + Brº Br2 (rate constant ke) Which of the following is true? The rate constant for the termination step is ka. The steady-state...
Draw out a stepwise mechanism (use fish hook arrow) for the reaction, including the initiation, propagation and termination steps in the peroxide-initiated hydrobromination of 2-Methyl-2-butene. Draw a stepwise mechanism (initiation, propagation and termination) for the following reaction:
Draw a plausible reaction mechanism for the following radical reaction. Include the initiation, propagation and termination steps. (5 points) 7. Cl hv +C-C +HCI
For the following reaction give the detailed mechanism in terms of: electron flow energy diagram, put both propagation step 1 and step 2 on the same diagram CH3--CH3 + Br2 ------> CH3CH2--Br + HBr This is what I have so far, and I think I'm correct. Im having trouble with the energy diagram. Initiation Br--Br ---> 2 Br . (dot symbolizes radical) Propagation (step 1) Br . + H--CH2--CH3 ---><---- Br-H + . CH2--CH3 Propagation (step 2) . CH2--CH3 +...
please show proper initiation and propagation mechanism 62) Which of the following is the best synthesis of 1, 1-dibromopropane, Br CH3CH2CH ? Br Br2 CH3CH=CH2 CCl4 Br2 light 2 HBr B) CH3CH=CH2 C) CH3C=CH 2 HB: D) CH3C=CH peroxide CH3CH=CH2 Brz E) H20
Write a mechanism for each of the following reactions. Clearly label the initiation,propagation, and termination steps in each reaction. 1. The light-initiated reaction of cyclohexane with chlorine to give chlorocyclohexane. 2.the reaction between cyclobutane and bromine to give bromocyclohexane. 3. The reaction between bromine and propane. 4.the reaction between bromine and cyclohexane to give bromocyclohexane.