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- Draww all possible organic products and kinds of reactions (SN1, SN2, E1, E2)Determine the reagents required for the following syntheses. More than one reaction is likely required. a) b) c) d) OH OH olm NH₂ MeO NHMe Me. Me OH OHDraw the structural formula for the major product of the following reactions.
- 9) Draw the conformer structure, Newman projection, before elimination and the elimination product of the following reaction: Br CH3ONA HA single alkyl bromide reactant theoretically yields either of the given products, depending on the reaction conditions. Draw the structure of the alkyl bromide compound. alkyl bromide (one compound only) CH, ОН СH O DMSOWhat is the organic molecule X of the following acetal hydrolysis? Please draw a skeletal line structure and include a detailed explanation and drawing of how the mechanism proceeds. Please include any relevant information that is needed to understand the process of acetal hydrolysis.
- Provide the reactant for the following reaction. Ph;P-CHCH3 O 1) cyclohexanone O 2) cyclohexanecarbaldehyde O 3) cyclohexylpropanone O 4) 3-cyclohexylpropanala,B-Unsaturated aldehydes and ketones can undergo reaction with nucleophiles at the B carbon, as shown below. Draw a resonance form for the unsaturated carbonyl that accounts for this reactivity.o Predict the two major organic products of the reaction. (HI behaves as an HX reagent.) H₂C ΤΟ + CH3 H—I CH3 Draw the two major organic products. H₂C H H CH₂ CH₂
- A) what is the major product formed (A-D) b) name the mechanism by which the major product is formed c)Which alcohol will form the most stable carbocation? CH3 a) CH;CHCH,OH CH3 b) CH—сон CH3 c) - OH d) CH;OH O a O b O d Organic compounds that contain terminal carbonyl group. ketone aldehyde ether alcoholDehydration of 1,2,2-trimethylcyclohexanol with H2SO4 affords 1-tert-butylcyclopentene as a minor product. (a) Draw a stepwise mechanism that shows how this alkene is formed. (b) Draw other alkenes formed in this dehydration. At least one must contain a ve-membered ring.

