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- The reaction below is classified as: a) substitutionb) eliminationc) additiond) rearrangementPlease provide the answers in each situation. 1. Which compound/s will react with Br2 in water under light conditions? (answer may be one or more) 2. Which compund/s will react with I2 in KI under dark conditions? (answers may be one or more)a) Draw the mechanism, using good curved arrow notation, for the reaction of 2-methyl-2- butene with bromine in water, omitting any stereochemistry: b) (R)-3-butyn-2-ol is treated with 2 mol of HBr, yielding optically active Compound A (C4H8OBr2). Draw the structure of the reaction with the correct stereochemistry. c) Name Compound A above, including stereochemistry. d) Compound A is treated with HBr to yield Compound B (C4H7Br3). The resulting solution is optically inactive. Draw the product(s) obtained and explain why there is a loss in optical activity.
- 1. Draw the organic product (ignoring stereochemistry) 2. State whether the process is overall oxidation, overall reduction, or neither.Please explain it. For each stereoisomer, draw the interconversion of chairs and identify the most stable. Give handwritten answer. ASAPWhen the optically active compound shown below reacts with HCl, two major products are formed: one optically active, and the other optically inactive. Draw each product. Which product is major?
- 1. SN1 or SN2 2. Include major product and stereochemistry 3. Add detailed reaction mechanismsDraw the mechanism ffrom benzaldehyde to this using: i)NaBH4 ii)TsCl, py iii)NaCN iiii)H+, H2O1. What are products formed from the below reaction? 2. Draw the stereoisomers and name them. Hint: There are two different constitutional isomers and each constitutional isomer has 2nstereoisomers.
- Rank the compounds in each set from most to least reactive in an EAS reactionWhat are products formed from the below reaction? Draw the stereoisomers and name them. (There are two different constitutional isomers and each constitutional isomer has 2^n stereoisomers.) Please solve the problem in detail.for the Cl2 addition reaction with 1,2dimethylcyclohexene, draw the most reasonable curved arrow mecanism. based on the reaction products, explain why a carbocation intermediate cannot be proposed