the duulatur nucleophile after rearrangement. This is the pluu If the carbocation Is captured by the...
answer all questions 1. For the following substrates, predict whether a carbocation rearrangement will take place in an SN1/E1 mechanism by first drawing the carbocation intermediate, then deciding if the carbocation will rearrange (can it form a more stable carbocation by hydride or methyl shift?): Carbocation: Sturcture Rearrange? If yes, draw the rearranged product. If no, write No н.с Br Н,с, Cн, 2. For each pair of nucle ophiles, circle which will react faster with CHsl in an Sx2 reaction....
need help with 1-21 1) Label the steps below as "slow" and "fast". HCH 013 10 = H. C + + H-LG H-LG 2) Why are they slow/fast? Explain using chemical terms. Stereochemistry of the Sn1 reaction 3) What type of intermediate does the Sn1 reaction proceed through? 4) What is the geometry of the carbon that the nucleophile coordinates to in the 2 step? 5) From how many directions would it be reasonable for the nucleophile to approach the...
Please, make the answer clear and reable. BrEtOH a OEt Hace H2C Alkyl halides undergo nucleophilic substitution and elimination reactions. When the kinetics of the reaction are measured, if the rate of the reaction is found to be dependent only upon the concentration of the alkyl halide the reaction is first order. The substitution reaction is thus termed ction is termed E1. These reactions are unimolecular and occur in two steps. The first step is rate-limiting and involves the loss...
need help with the boxed bullet point. writing the chemical reaction scheme for the experiment. Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part I Pre-lab Assignment for Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part 1 1. From The Organic Chem Lab Survival Manual ( edition) by Zubrick • Review pages 201-204: Standard Reflux. • Review pages 127-140: Extraction • Review pages 164-189: Distillation, Simple Distillation. The Distillation Example, and The Distillation Mistake. 2. Read this...