12. Solvolysis of the compound below in methanol gives a complex mixture of three compounds. Give...
7) Solvolysis of bromomethylcyclopentane in methanol gives a complex mixture of the following five compounds. Propose mechanisms for compounds a,b and c to account for these products. (12 pts) A B C
Solvolysis of bromomethylcyclopentane in methanol gives a complex product mixture of five compounds. Propose mechanisms to account for those products.
(1pt) Give the substitution product expected from solvolysis of the compound shown below by heating in ethanol. 3. OTS
please explain your answers 6-40 Give the substitution products expected from solvolysis of each compound by heating in ethanol. (b) C (e) Br (d) solod Bror CH3 Br
8.1) 8.5) Give the appropriate IUPAC name for the following structural formula of a halogenated compound. CH3 CI Нас (Where stereochemistry is shown, include a designation of configuration in your answer. Use cis/trans designations only to represent stereochemistry for cyclic compounds. It is not necessary to use italics in writing compound names.) Name: There are five cycloalkanes with the molecular formula C5H10. When treated with chlorine at 300°C, isomer A gives one monochlorination product. Under the same conditions, isomer B...
(i) Give reaction mechanisms that account for the observation that all three solvolysis reactions gave the same ratio of the three alcohol products. Aci EtOH/H20 dº 2040 EtOH/H, 204 0". anon ЕТОН/Н,0 Wci [5 marks]
Three isomeric ketones, compounds A, B, and C, with the molecular formula C_7H_14O are converted into heptane by Clemmensen reduction. Upon Baeyer-Villiger oxidation, compound A gives a single product; compound B gives two different products with very different yields; compound C gives two different products in virtually a 1:1 ratio. Deduce and draw A, B, and C in the labeled boxes below. Incorrect. The ketone you have drawn as compound B does fit the molecular formula and produces heptanes upon...
I have a mixture of three compounds and I want to separate them. The compounds are ethyl aminobenzoate (50%), benzoin (40%), and 1,4-dibromobenzene(10%). I started the experiment by dissolving the mixture in the methylene chloride, then I added HCl, so I got two layers, first one is aqueous layer that contain ethyl aminobenzoate, and the second one is organic layer that contain benzoin and 1,4-dibromobenzene. After that I add NaOH to aqueous layer and I got a solid, then I...
3. Shown below is a compound that is soluble in methanol (CH3OH). Show how methanol would act as a solvent for this compound (show two methanol molecules, one acting as an acceptor and the other acting as a donor). Lone pairs of electrons are should be shown on all atoms that contain them. A complete answer would include drawing the Lewis structure for the compound shown below H_CC(CH3)OCH(OH)NH2
please help with organic chemistry! mechanisms? 5) The reaction of 2-bromo-1,1-dimethylcyclohexane with methanol gives the following products. Please provide a detailed explanation to the formation of each product. You should use structures of intermediates in your answer. (8 points). осн, CH,он OCH Br + 6) There are a variety of isomeric 1,2,3,4,5,6-hexachlorocyclohexanes, but one of them does not react with CH3CH20' to give an elimination product. Provide the structure of this compound and briefly explain why it does not react...