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Subject- chemistry
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Solved in 3 steps with 2 images
- 1.)How is this reaction is carry out ? Show all the steps please arrows and all the movement of electrons. 2.)Show the Jones intermediarycan someone pls help me find the product of thisThis is a question from a study guide for o-chem. If you can please go though the difference between a major and minor product and help me break down the reaction a bit id really appreciate it.
- (a) Analyze SN1 or SN2 is preferred in the reaction below. Explain your choice and express themechanisms.The Br produced by the reaction in Figure 9.2 could combine with the carbocation you drew to give a dibromide product (a product with two Br atoms). Use a curved arrow to show the Br making a bond to the carbocation, and draw the resulting dibromide product.Carefully solve the major product of each reaction and show the steps of the process.
- Why 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.1. Which of the following is the strongest nucleophile? Refer to the diagram below with an MeOH, MeSH, etc. 2. Which of the following is true about the stereochemistry of SN1 reaction?a.retention of configuration at the electrophilic centerb.50:50 mixture of retention and inversion of configuration at the electrophilic centerc.inversion of configuration at the electrophilic centerd. slightly more inversion than retention at the electrophilic centerPlease help with this ochem mechanism... 1. Provide the stepwise mechanisms of the given reaction a) o,p-dinitrochlorobenzene + NaOH