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- 1 Produce the given molecules from-any simple alkyl halide consisting of 4 or less carbons or (use no other functional groups other than these, ethylene oxide, cyclohexane, or cyclopentane. Any other carbon- containing reactants must be synthesized from the reagents gave above... Please explain too!!The hydrobrominationof 2-methyl-1-butene could theoretically lead to 2 different alkyl bromides; in practice only one product is formed. Draw the structure of both theoretical products, circle the one that is actually produced, and briefly explain whyonly one product forms.Drawing Hydrohalogenation with a Carbocation RearrangementDraw a stepwise mechanism for the following reaction.
- Identify F in the following reaction sequence. F was converted in several steps to the antidepressant paroxetine (trade name Paxil; see also Problem 9.9).The reaction below could run through both substitution and elimination reactions. 1. Provide the correct reagent to produce the products shown 2. State which mechanism(s) was followed1. SN1 or SN2 2. Include major product and stereochemistry 3. Add detailed reaction mechanisms
- Below is a schematic representation of possible reactions that Compound X can undergo. Use the scheme to answer the following questionsA)What is the IUPAC name for Compound X?B)What type of reaction (s) is/are represented by (i) and (ii)?C)Compound X undergo transitions through either [A] or [B] to produce compounds [1], [2], [3] and [4]. Draw the structures of [A] and [B]. D)Illustrating with reaction mechanisms, show how compounds [1], [2], [3] and [4] are formed.E)Which of the compounds in the following pairs will occur in relatively higher yields and why?I)[1] and [2] II)[3] and [4]Compounds A, B, and C have the same molecular formula C4H8. They all react wotu H2/PtO2 to give the same compound. The reaction of A or B with H2O/H2SO4 or with BH3-THF, followed by treatment with a basic solution of hydrogen peroxide, gives the same compound, namely D. The reaction of C with H2O/H2SO4 also gives D. However, the reaction of C with BH3-THF, followed by HO-, H2O2 gives a new compound, E. Provide the identity of A, B, C, D, and E along with explanations of reactivity.Draw the ALL of the E2 organic product formed when the structure shown below undergoes dehydrohalogenation in KOH with heat.
- Answer the following question about curcumin, a yellow pigmentisolated from turmeric, a tropical perennial in the ginger family and aprincipal ingredient in curry powder. Most enols, compounds that contain a hydroxy group bonded to a C=C, are unstable and tautomerize to carbonyl groups. Draw the keto form of the enol of curcumin, and explain why the enol is more stable than many other enols.a,B-Unsaturated aldehydes and ketones can undergo reaction with nucleophiles at the B carbon, as shown below. Draw a resonance form for the unsaturated carbonyl that accounts for this reactivity.-Give the correct mechanism via correct arrow pushing -name each mechanism -name each major and minor products (1S,2S)-1-iodo-2-methylcyclohexane with KOH/DMSO-->