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- Can you assit with confirming product(s), define major/minor, show stereochemistry, if appropriate, and/or if no reaction occursDraw the main organic products of the reaction. Indicate the stereochemistry, including all hydrogen atoms, at each stereocenter. Omit byproducts such as salts or methanol.Consider compound I below, which is structurally related to a natural product that was isolated from an extract of a Caribbean marine sponge (See J. Chem. Soc. 1994, 116, 6015). Answer the following questions about this compound (please explain answers) How many double bonds with E stereochemistry are present? _________ How many double bonds with Z stereochemistry are present? _________
- A. For each reaction1) Provide the missing reagents/conditions or major organic products as appropriate2) Assign each reaction as Oxidation or Reduction unless otherwise directed3) Pay attention to stereochemistry including racemic mixtures unless specifiedThe following compound readily eliminates CO; to form a conjugated six membered ring. (a) Complete the reaction with drawing the possible structure and (b) explain why this reaction goes steadily.(A) Provide the major organic product for the reaction below (B) Would the product be optically active of optically in active?
- - Identify compounds J & K - Draw a curved arrow mechanism that accounts for the formation of J (take into account stereochemical considerations)Bromide Bhas normal activity (for a secondary bromide) towards SN1 substitution, but A has much higher reactivity and Chas much lower reactivity.(a) Why cyclohexene and cyclohexa-1,3-diene are expected to undergo addition reaction but benzene does not? Explain clearly. (b) Why is an electron-donating group to benzene activating and usually a/an ortho/para director?
- Rank A, B, and C in order of increasing SN1 reactivity.Draw the structure(s) of the major organic product(s). -Show stereochemistry where appropriate -No rxn is a possible optionA) Show full rxns/mechanisms with major product/s Aniline with SO3 in H₂SO4 catalyst Benzoic acid with Br₂ and FeBr3 catalyst Nitrobenzene with CH3CH2Cl and AICI3 catalyst o-xylene with H₂ in Rh/C catalyst tert-butylbenzene with aqueous KMnO4 See PHOTO.