A Br FeBr3 2 -Li then H30* D LIAIH4 then H3O* Propose reaction conditions (A) and draw the products (B, C and D) of each transformation. Curve arrow mechanisnms are not required

Q: ism of ving eactions. а) OBr Br OtBu HOtBu b) HH H HOtBu OtBu CI CI c) H3O H20

A: Since you have posted question with multiple subparts as per guidelines we can solve only one per…

Q: ဝ a) H3NCHCNHCH₂CO₂ CH3 -N=C=S 1) NaOH 2) anhydrous CF3COOH 3) aq HCI HN- H CH3 CI + Hဒ္ဒNCH၇CO2H

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Q: Pls help ASAP on both questions I HUMBLY REQUEST

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Q: 1. Using curved arrows, draw the mechanism of the following reactions: a) catalytic H* N-R1 H,N-R R…

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Q: 3. Draw a complete mechanism for the reaction below. Start by include all lone pair electrons, then…

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Q: Synthesis? - H-=H Mechanism? Intermediate Products included Br HB-, H₂021A Br

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A: The reaction shown is an example of nucleophilic substitution reaction following SN1 mechanism.

Q: 8) Provide the major organic product(s) of the reaction shown below CH3CH₂COCI, AICI, 9) What is the…

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A: The missing reagents and products can be shown below,

Q: None

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Q: 5. Identify the necessary to accomplish the 2-step transformation below.

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Q: 7. Using curved-arrows, transformation stereochemistry propose a mechanism for the following and…

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Q: A B Br FeBr3 1 =Li then H30* D LIAIHA then H30* 2.

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Q: Reacti on Scheme:2ndrxn Ha sula (care) + Hzo HO n-butano I acetic acid n-buty acetate

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