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- 1. what is the Nature of the leaving group (LG)? 2. what is the relative size of activation energy (Ea) for each reaction? 3. what is the Hammond's postulate? 4. what are the Relative thermodynamic stability of the reactive intermediates? 5. what is Influence of the solvent (if given) on the reactions and intermediates?Chemistry please provide the flow of electrons aswell!! thank you! using the starting material (on the left) to determine the sythetic route which will be the most reaosnable and effective to theres none, you have to start witth the begin products to get to finish needed by using the minmium reagents and reactions needed to get to the final productFor SN2 Explain if 3o ( tertiary) alkyl halides reacted (fastest or slowest) explain why. Be sure to explain if alkyl halides did not react or did react and why. 3o (tertiary) compounds listed are: 2-chloro-2-methylpropane (see picture) Base your explanations on the following considerations: the nature of leaving group, the effect of structure, steric hindrance and any other feature.
- Can someone explain the answers to 28, 29, and 30? The answers are B, A, A. I understand lindar catalyst makes cis alkenes and Na/NH3 makes trans alkenes but I dont understand how the second step of Br2, OsO4 influences the stereochemistry between the 2 . Will rate quickly if helpful. Thanks!Please help with the following ochem mechanisms.... 1. Provide the stepwise mechanisms for the following reactions (see attached picture)i need help filling out the following SN2 reactions with appopiate reactants, products, or reagents,
- Show the SN2 mechanism in the reaction between (S) 2-bromobutane and iodide ion. Label the product and draw a enery diagram for this reaction.Provide the synthetic route for the following reaction? (CH3)2CHCH2Br ----> (CH3)2CHCH2CH2CH2NH2Below 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?
- Please help me with the a proposed Williamson ether sysnthesisi for 3-ethoxyhexane. Thank you !Draw the final product of the third step after treatment with KMnO4, KOH, and heat followed by aqueous acidic workup.Can you pls assist me with the mechanism of Benzyl alcohol being oxidised to Benzyl aldehyde and to Benzoic acid using KMnO4 as an oxidant. Showing arrows and everything.