Draw the structure of the alkyl bromide and the nucleophile that will react in an Sx2 reaction to give the product shown. CN Alkyl bromide - Nucleophile H3C
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- Draw the structure of the alkyl bromide and the nucleophile that will react in an Sy2 reaction to give the product shown. Alkyl bromide + Nucleophile -C=CH You do not have to consider stereochemistry. Separate multiple reactants using the + sign from the drop-down menu. opy aste C ChemDoodle >2. Draw the structures and explain why CH3CH₂O and CH3CO₂ are good nucleophiles but CH3SO3, water, and alcohols (R-OH) are poor nucleophiles. Propose a 'cutoff' for the amount of negative charge needed to be a good nucleophile. CH3CH₂O CH3CO₂ CH3SO3 H₂O CH₂OHShow how you might synthesize this compound from an alkyl bromide and a nucleophile in an S№2 reaction. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Only draw the reactants. Separate multiple reactants using the + sign from the drop-down menu. • If there is more than one possible combination of alkyl bromide and nucleophile, draw only one combination. • Do not include counter-ions, e.g., Na+, I, in your answer. / CN Submit Answer TAYY ? ChemDoodle Ⓡ Retry Entire Group • #[ ] در 7 more group attempts remaining
- Show how you might synthesize this compound from an alkyl bromide and a nucleophile in an S№2 reaction. N3 • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Only draw the reactants. Separate multiple reactants using the + sign from the drop-down menu. • If there is more than one possible combination of alkyl bromide and nucleophile, draw only one combination. • Do not include counter-ions, e.g., Na+, I, in your answer. 90-85 TAYY ? ChemDoodle O OO. #[ ] درShow how you might synthesize this compound from an alkyl bromide and a nucleophile in an SN2 reaction. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. Only draw the reactants. Separate multiple reactants using the + sign from the drop-down menu. • If there is more than one possible combination of alkyl bromide and nucleophile, draw only one combination. • Do not include counter-ions, e.g., Na", I, in your answer.In the reaction series below, write down the appropriate reagents that can be used where there are question marks.
- Rank in terms of reactivity towards the nucleophile. 1=least 4=mostShow how you might synthesize this compound from an alkyl bromide and a nucleophile in an SN2 reaction. N3 • Use the wedge/hash bond tools to indicate stereochemistry where it exists. Only draw the reactants. Separate multiple reactants using the + sign from the drop-down menu. • If there is more than one possible combination of alkyl bromide and nucleophile, draw only one combination. Do not include counter-ions, e.g., Na", I", in your answer. opy astePlease answer the two items. The following compounds are major products of an elimination reaction with an alkyl halide. Determine the structure of the alkyl halide. Write the overall reaction mechanism. Tip: Remember your Markovnikov’s rule. Follow the progress of the reaction and look at the stability of the intermediate products and transition states to determine the minor and major products.
- The addition of an alcohol to an acid chloride is an example of alcoholysis (alcohol addition with bond breakage). Consider the alcoholysis reaction below and answer the questions that follow. 1. Show the tetrahedral intermediate that is formed after the nucleophilic addition of the alcohol to the acid chloride. Be sure to include all lone pair electrons and formal charges on your intermediate structure. 2. Show the final product of this alcoholysis reaction that forms after the intermediate you made in Part 1. Do not include inorganic or charged products in your answer. Be sure to include all lone pair electrons and formal charges.4. Complete the phrases with one or more of the following terms: SNI, SN2, E1, E2. a) The reaction takes place in two or more steps. b) The reaction goes through a carbocation. c) The rate determining step has two reactants. d) The rate is independent of the concentration of nucleophile or base. e) Zaitsev's rule is often applicable to the products..Polar aprotic solvents enhance the rate of an SN2 reaction by stabilizing the cations and the anions. changing the polarizibility of the nucleophile. raising the energy of the nucleophile. O lowering the energy of the nucleophile. Save for Later