Draw the structure of the missing reactants, intermediates, or products in the following mechanism. Include all lone pairs except on metal atoms. Ignore stereochemistry. Ignore inorganic byproducts. CH, H- 0: Hg(OAc)2 Draw Starting Alkene
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- Please identify priorities of functional groups and name following molecules based on thier stereochemistry as R or S1-methylcyclohexene is reacted with the following reactants. Write products. Write which stereochemistry is valid (syn/anti, racemization, antimarkovnikof, etc). 1- Br2/ H2O 2- CH2N2/heatExplainwhythefollowingdeuterated1-bromo-2-methylcyclohexaneundergoes dehydrohalogenation by the E2 mechanism, to give only the indicated product. Two other alkenes are not observed.
- When 2-cyclobutylpropan-2-ol is treated with a solution of HBr in Et2O, 2-bromo-1,1-dimethylcyclopentane is the resulting product. Write the reaction and propose a mechanism using curved arrows notation in each step.Draw all of the substitution and elimination products formed from thegiven alkyl halide with each reagent: (a) CH3OH; (b) KOH. Indicate thestereochemistry around the stereogenic centers present in the products,as well as the mechanism by which each product is formed.Draw mechanism arrows and then predict the major products and stereochemistry. Also include the labels of thermodynamic and kinetic 3,4-dimethylhex-3-ene with HCl
- Draw the major organic product(s) for each reaction below. Indicate the stereochemistryDraw mechanism arrows and then predict the major products and stereochemistry. Also include the labels of thermodynamic and kinetic no stick structure don't understand 3,4-dimethylhex-3-ene with BH3. After reaction is complete, add H2O2, –OH, and H2ODraw the major organic product(s) for each reaction below. Indicate the stereochemistry where necessary, clearly with wedges or dashes.
- cis-4-Bromocyclohexanol and trans-4-bromocyclohexanol form the same elimination product but a different substitution product when they reactwith HO-. a. Why do they form the same elimination product?b. Explain, by showing the mechanisms, why different substitution products are obtained.c. How many stereoisomers does each of the elimination and substitution reactions form?Addition of hydrochloride acid to 1-isopropenyl-1-methylcyclopentane generates 1-chloro-1,2,2 trimethylcyclohexane. Draw the complete mechanism, including intermediates, to illustrate electron flow in the reaction.Draw the arrow-pushing mechanism and propose the products. When appropriate, make sure to indicate the appropriate stereo-/regio-chemistry of the product(s). Note that the mechanism(s) by which the product(s) form in reactions A and B are shown in pink. For Reactions C, D, and E you need to deduce the mechanism by carefully analyzing yout reagents and conditions.