Draw the SNl or SN2 reaction with CN for the following molecules t butylchloride , n - butylbromide , 2 -bromobutane . Explain in which mechanism it will react and why ?
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- 3) Explain how and why the reaction below results in the observed regiochemistryand/or stereochemistry.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.Which compounds from 5a-d will react with hydroxide in the fashion shown. Which reaction will be the fastest and slowest? Explain using knowledge of carbonyl chemistry, pka and leaving groups.
- Why does the final product has the opposite configuration compared to the reactant? Shouldn’t it form OMs first, then OMs gets substituted by Cl- via Sn2 (the 1st inversion of configuration) then the Cl- gets substituted by OCH3- (the 2nd inversion of configuration? To my understanding 2 inversions = same configurationHow do you properly write an SN1 reaction, with transition states/intermediate steps included?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?
- a. What are the products of following reaction?b. Write the reaction mechanism for each using the right arrows and define it as Sn2, Sn1, E2 or E1.c. Explain why do you choose that product and mechanism or in case something else happens explainwhy.For SN1 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.Draw all possible alkenes that could be generated from an E2 elimination reaction of 3-bromo-3-methylhexane. Suggest conditions that can be used to make just one of the alkenes in a controlled manner (i.e., conditions that would lead to formation of just one alkene as the major product).
- Complete the reactions given below, write down the type of mechanism (SN1, SN2, E1, E2)?Draw the mechanism ffrom benzaldehyde to this using: i)NaBH4 ii)TsCl, py iii)NaCN iiii)H+, H2O1.Draw the product, please shows step by step in details 2.Explain if (CH3)2CH in this reaction can attach in ortho positon in Friedel Craft Alkylation?? why or why not???