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What is the expected major product of reacting cyclohexane carbaldehyde jwith CH3NH2?
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- What is the expected major product of reacting cyclohexane carbaldehyde with (CH3)2NH?What order of reagents should be used to synthesize the following product from methylcyclopentane?(A) Br2(B) Br2, hv(C) KOH, heatWhat is the major product formed when 3-methyl-1-butene is treated with Hg(C2H3O2)2 in a THF/ethanol mixture followed by NaBH4 in base?
- Draw all products of the reaction of (1S,2R)-1-bromo-1,2-dimethylcyclohexane in 80%H2O/20%CH3CH2OHat room temperature..Q7 Consider the reaction, where the alkane shown is subjected to radical bromination at 25 °C. Br₂ light Describe the major monobromination product. productAs a rule, axial alcohols oxidize somewhat faster than equatorial alcohols. Which would you expect to oxidize faster, cis-4-tert-butylcyclo-hexanol or trans-4-tert-butylcyclohexanol? Draw the more stable chair conformation of each molecule.
- Two products are formed when methylenecyclohexane reacts with NBS? Show how each is formed. Disregard stereoisomers.Account for the regioselectivity and stereoselectivity observed when 1-methylcyclopentene is treated with reagent Q.Hg(OAc)2 in H2ODraw the major product formed when HBr reacts with the following epoxide. Use wedge/dash bonds, including H's at each stereogenic center, to show the stereochemistry of the product.
- Draw all of the substitution and elimination products formed from thegiven alkyl halide with each reagent: (a) CH3OH; (b) KOH. Indicate thestereochemistry around the stereogenic centers present in the products,as well as the mechanism by which each product is formed.Q2. What are the products of the following reactions? Q3. 2-Bromopentane, when treated with alcoholic KOH yields a mixture of three alkenes A, B and C. Identify A, B and C. Which is predominant? Draw the product of the reaction of 1,2-dimethylcyclohexene with [math]H_{2}[/math] over a Pd catalyst. Show stereochemistry with wedged and dashed bonds.