Yead.III. Show a complete synthesis of the following molecule starting with cyclohexane (as many times as you wish), anymolecules of three (3) carbons or fewer, and any other reagents. (16 pts)Zoxo5BrBV-Br+BrHBVBr-BrBrBr BrBrBrHBVBrBrBrz←·Br BrBLΔHGHO)TH F-OHонして

1. Hydrogenation of Benzene: In the presence of a platinum catalyst, hydrogen gas reacts with…

Answered: Yead. III. Show a complete synthesis of…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter13: Substitution

Section: Chapter Questions

Problem 4E

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Propose mechanisms compatible with 1) and 2) of the following reactions.
Explain why the following reaction is not a good way to prepare 1-phenylpentane: benzene + 1-chloropentane + AlCl3 → 1-phenylpentane In your scratch work, give the full, curved-arrow mechanistic explanation of what would happen, and indicate what would likely be your main product or products.
Propose a suitable mechanism based on the observation .
Give detailed answer- Provide example of compound that fulfil each criteria below. Explain why-A)1,2-disconnectionB)1,4-disconnectionC)1,5-disconnectionD)1,6-disconnection
For butenafine, develop a synthesis that starts with napthalene and benzene. (aromatic methyl groups can be converted to alkyl bromides using Br2/light, and aldehydes by heating the alkyl bromide in DMSO, eg. ArCH3 to ArCH2Br then to ArCHO).
please provide the machanisms of 1a, 1e, 1f
Please help. Questions in images. Solvent Rf of A Rf of B Rf of C 10% ethyl acetate-90% hexanes .12 .07 .01 20% ethyl acetate-80% hexanes .34 .29 .10 30% ethyl acetate-70% hexanes .53 .42 .22 40% ethyl acetate-60% hexanes .72 .61 .35
QUESTION- Label these spectra attached. Use them to discuss differences in reactant and product spectra that determine/support positive product formation. please no general responses, be specific to peaks in the spectra attached. EXPERIMENT: Synthesis of Benzil - Multi-Step Synthesis Part B benzoin + NH4NO3 ==== benzil ReferencesLehman, J.W. Operational Organic Chemistry: A Problem- Solving Approach to the LaboratoryCourse, 3 rd Ed., Prentice-Hall, Inc: New Jersey, 1999, p. 449.
In the following three compounds(1,2,3) arrange their relative reactivity towards the reagent CH3Cl / AlCl3. Justify your order?
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For SN1 Explain the order in which 2o (secondary) alkyl halides reacted (fastest to slowest) and explain why. 2o (secondary) compounds listed are: (see picture) 2-chlorobutane 2-bromobutane bromobenzene bromocyclopentane bromocyclohexane Base your explanations on the following considerations: the nature of leaving group, the effect of structure, steric hindrance and any other feature. Be sure to explain which alkyl halides did not react and why
(a) A compound known to be a substituted cyclohexanone derivative has lamda max of 235 nm. Could this compound be a conjugated dienone? explain (b) (i)For this compound, how many nm must be accounted for by substituents? (ii) What are the substituents and the points of substitution that may occur having accounted for the 20nm?

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