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- Synthesize isopropylcyclopentane from alcohols having ≤ 5 C's.Draw all products of the reaction of (1S,2R)-1-bromo-1,2-dimethylcyclohexane in 80%H2O/20%CH3CH2OHat room temperature..Cyclohexene plus 1) Hg(OAc)2, H2O; 2) NaBH4; yields __________. HO2CCH2CH2CH2CH2CO2H a cyclic diketone cyclohexyne cyclohexanol OHCCH2CH2CH2CH2CHO
- How would you synthesize the following compounds from cyclohexanone? a) 1Methylcyclohexene b) 2Phenvlcyclohexanone c) cis1, 2Cyclohexanediol d) 1CyclohexylcyclohexanolTreatment of p-bromotoluene with NaOH at 300°C yields a mixture of two products, but treatment of m-bromotoluene with NaOH yields a mixture of three products. Explain.Identify all possible product(s) in the following reactions. a) 1-bromocyclohexane with sodium hydroxide.b) 2-chloro-2-methylpentane with water
- We are asked to prepare (CH3)2CHCH2OH (2- methylpropan-1-ol) from an alkyl halide and any required reagents ?What product do you expect from the reaction of the following etherswith HBr? a. CH3CH2OCH2CH3 b. cyclohexyl ethyl ether3H. Put it all together. Predict the E1 products of the following reaction. Label alkenes as E/Z. 4. Predict the E1 products of the following reaction. Label akenes as E/Z.
- The pKa of p-cyclopropylbenzoic acid is 4.45. Is cyclopropylbenzene likely to be more reactive or less reactive than benzene toward electrophilic bromination? Explain.What is the expected major product of reacting cyclohexane carbaldehyde jwith CH3NH2?a. Draw the major product(s) of the reaction of 1-methylcyclohexene with the following reagents, disregarding stereoisomers: 1. NBS/Δ/peroxide 2. Br2/CH2Cl2 3. HBr 4. HBr/peroxide b. For each reaction, show which stereoisomers are obtained.