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- Molecular halogen (X2) adds to alkenes to make vicinal dihalides. In the boxes, draw thecurved arrow notation for the reaction.What steps are needed to convert Y to the alkene Z ?(b) Consider the reaction of 1-bromobutane with a large excess of ammonia (NH3). Draw the reactants, the transition state, andthe products. Note that the initial product is the salt of an amine (RNH3+ Br - ), which is deprotonated by the excess ammonia to give the amine.
- Find out what kind of reaction each alkene goes through. Figure out what the main products of each equation will be. Draw these things and name them.Having trouble and the answer I put is wrong. Name the alkene below.Use ONLY E/Z designators to indicate stereochemistry.The reactants, intermediates, final products, and all curved arrows showing bonds forming andbreaking are collectively referred to as the mechanism of a reaction. For the following reactants: a. Explain why the original statement of Markovnikov’s rule does not help in this case, but themodern restatement of Markovnikov’s rule tells you which carbon will get the X (Cl). b. Show the mechanism of the most likely addition reaction between the reactants.
- H2. Please show proper step by step explanation and also explain wrong optionsorganic chemistry help Fill in the missing starting materials, reagents, or major products of each reactionReplacing a kin, a word each of the following our kids results in a significantly lower reaction. Identify the reasons for this decrease in rate for each alkene D – F. Select all that apply.