The reactant alkane react with Br2 by radical substitution under photochemical or UV light, the alkyl halide and HBr are formed. In general the alkane free radical reactivity order is tertiary > secondary > primary > methyl. The reaction proceeds via radical chain mechanism which involves radical intermediates following two key steps mechanism.
Step 1: Radical initiation process
Under the uv light, the weak halogen bond to undergo homolytic cleavage to generate two bromine radicals and starting the chain process.
Step 2: Product formation process
A bromine radical abstracts a hydrogen from the starting reactant alkane to form HBr and the tertiary alkyl radical which abstract a bromine atom from another molecule of Br2 to form the desired product as alkyl bromide and another bromine radical.
The reaction mechanism of the given reaction is explained in the below image.
help please OPT, 10PT EA): Provide the mechanism for the to nanism for the following transformations...
3. MECHANISM (20PT, 10PT EA): Provide the mechanism for the following transi following transformations Br2, hv w EtOH OEt
V2 Q9. Provide reagents for the following transformations 0 CI Provide a stepwise mechanism for the formation of the major product in the following free radical bromination reaction. All steps and intermediates (as well as arrows leading to it) must be shown. Show formation of bromine Br2 (10 points) +HBr NBS, hv 0 Initiation: Propagation Termination Best Wishes! G.Sathianathan
Provide a detailed mechanism for the following transformations.
5. (6 points) Please provide a step-by-step mechanism for the following transformations. Ol. (H+) .
Please provide the mechanism for the following transformations. Identify type SN1, SN2, E1, OR E2. Ots t Nal tone
I need the mechanism please. IV. Provide a complete stepwise mechanism for the following reaction sequence, including initiation and termination steps for any radical reactions (i.e. write a continuous reaction mechanism with the product of step 1 being used in step 2.... Draw the product of each step in the indicated boxes. 1) Br2, hv 2) KO Bu/BuOH 3) HBr, ROOR Br step 1 product step 2 product
URGENT Organic chemistry help - please show the mechanism. thank you!! 3.) What is the mechanism and main product for the following series of reactions? (5 points) 1.) Br2, hv 2) Na CN 3.)excess H30
7. Mechanism Cont'd: Provide the mechanism for both of the following transformations. 1. NaOM, MeOH H30* 2. H30
Provide a mechanism for the following reaction. Br2, hv H2 H2 CH - HBr H2 H2 H3C Br
2. For the following transformations, please provide detailed conditions to give the designated product in maximum yield with minimum by-products. More than one step may be needed. [8 pts ea] o OMe Phoн OH