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- Step 4a: Classify step. The target product is present, but the reaction is not over. The ethoxide ion has been regenerated. :0: :0: What is the key process in the next step of the mechanism? proton transfer formation of a o bond between nucleophile and electrophile loss of a leaving group carbocation rearrangement (e.g., methyl or hydride shift)Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. LOCH3 LOCH3 HNO3 / CH3CO₂H O₂N • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. ● In cases where there is more than one answer, just draw one.Draw the electron-pushing mechanism for the propagation steps of the allylic bromination reactions below. You may omit NBS in your mechanism, and use Br and Br2.
- Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. CI CI HNO3 / H2SO4 O2N You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one.Consider the reaction of NaCN with 1-bromohexane in DMSO. Predict the change in rate of reaction if the concentration of the NaCN is tripled. A) The reaction rate stays the same B) The reaction rate doubles C) The reaction rate is halved D) The reaction rate quadruples E) The reaction rate triplesDraw the product(s) for this reaction and state the reaction mechanism.
- Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. CI CI HNO3 / H2SO4 O₂N You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one. √n [ ?Draw the least stable resonance form for the intermediate in the following electrophilic substitution reaction. CEN Br₂/FeBra • You do not have to consider stereochemistry. Include all valence lone pairs in your answer. In cases where there is more than one answer, just draw one. Br CEN I1,3-Butadiene undergoes an electrophilic addition with HBr. Complete the steps in the mechanism to produce the product shown. 2) Draw both the organic and inorganic intermediate species. Include all nonbonding electrons and charges. Draw a curved arrow to convert the intermediate into the product shown. 1) Add curved arrows for the first step. -Br: H, :Br: Нзс -сн—CH2 н
- Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. CH3 CH3 CH3CI / AICI3 • H3C • You do not have to consider stereochemistry. Include all valence lone pairs in your answer. In cases where there is more than one answer, just draw one.i)State the type of reaction. (ii) What is the function of the sunlight in the reaction? (iii) Draw the structure of monosubstituted products, A and B. Label the major product. (iv) Draw the propagation steps in the mechanism for the formation of the major product.Draw the mechanism for the reaction