Draw a mechanism for the following reaction: H,C HC Br CH, H-Br CH H,C H,C Edit the reaction by drawing all steps in the appropriate boxes and connecting them with reaction arrows. Add charges where needed. Electron- flow arrows should start on the electron(s) of an atom or a bond and should end on an atom, bond, or location where a new bond should be created. H* EXP. CONT.
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- The reaction below could run through both substitution and elimination reactions. 1. Provide the correct reagent to produce the products shown 2. State which mechanism(s) was followedEnamines formed from the cyclic secondary amine pyrrolidine are important intermediates in the synthesis of 1,5-diketones. (1st pic) On the structures provided below, draw arrows showing electron flow for the reaction mechanism for the acetic acid-catalyzed formation of an enamine from cyclohexanone and pyrrolidine. (2nd pic)Below is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- Rate = k [CH3CH2Br][CH3COO-] Which mechanism would best fit the data?
- The replacement of CH3OH to dimethyl sulfoxide, DMSO (CH3)2S=O) as a solvent in the substitution reaction below results in what?Predict the product, draw the mechanism, and plot the reaction coordinate diagram for theE1 reaction.Below is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- ΔH=-75 kJ/mol Rate = k [CH3CH2Br][CH3COO-] Which reaction energy profile would be the best representative of the data provided?
- N(CH2CH3)3 + HNO3 --------> a.) rewrite the reaction using bond-line structure of reagents and products of the reaction b.) supply the curved arrows explaining the mechanism of the reaction2-butanol + NOx + hv (assume the carbon-hydrogen bond on the carbon adjacent to the carbonwith the alcohol group is the weakest) For each mechanism, provide the photolytic cycle, a source for hydroxyl radical (if needed) AND atermination step. You may stop when you have accounted for all radicals AND all VOCs are stable (i.e., ifformaldehyde is a product of your mechanism, you do not have to oxidize that molecule to).Draw the neutral organic starting material. The Hint: The reaction conditions support electrophilic addition of Br2 to an alkene's C=C double bond, which would normally yield a dibromo product. However, the product has only one bromine atom, with a C–O bond on the adjacent carbon. This fragment is diagnostic for a halohydrin, where an oxygen nucleophile (water or alcohol) reacts with a bromonium intermediate to generate the O–CH2CH2–Br motif. Work backwards to determine what the starting material must look like. There should be an alcohol and an alkene in the neutral organic starting material.
- Predict the major organic product formed when the compund shown below undergoes a reaction with H2O2 and then is heated in H2O. The 2nd photo is what I thought was the answer, but when I put it into Mastering Chemistry, it was counted as wrong and my feedback was, "What configuration is the C=C bond expected to haev?" I'm confused as to what this is referring to, so I appreciate any help given.(a) Analyze SN1 or SN2 is preferred in the reaction below. Explain your choice and express themechanisms.The following mechanism is given: . The first step is:• Protonation• Deprotonation• replace2.2. : B-particle represents:• The base• Nucleophiles• Electrophilic• Radicals2.3. The shape arrow indicates:• Equilibrium• Reversibility• Tautomeria• Transform2.4. The last step is:• Nucleophilic infestation on electrophilic• Electrophilic attack on the nucleophile• Attack of the oxygen atom on a double bond• Double bond splitting Please answer in detail, each step of mechsnism with suitable answer otherwise I'll downvote