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Question Propose syntheses of the following compounds beginning from a mono-substituted benzene. NH CH CN CH.CH...
37 Propose syntheses of the following compounds beginning from a mono- substituted benzene NH₂ CN b) CH₃ CH₂ CH₂ COH Br c) d) CI NH2
Propose syntheses of the following molecules, starting from benzene, toluene or phenol, any inorganic reagents and any organic reagent of TWO carbons or less: 4. Propose syntheses of the following molecules, starting from benzene, toluene or phenol, any inorganic reagents and any organi c reagent of TWO carbons or le a) NO2 b) CO2H c) OH d) e) NO2 NO2 Br CI CI CO2H Br
Please put all 6 steps. Design a synthesis of 2-bromo-1-chloro-4-nitrobenzene from benzene or any mono-substituted benzene. Cl Br benzene or any mono-substituted benzene NO2 Part 1 out of 6 Choose the best option for the immediate precursor to the target molecule. CI Br NO2
Propose syntheses of each of the following compounds, from the given starting material and any other needed reagents. » O- CH2OH from O con b) CH3CCHz from CH3CH=CH2 ОН • OCHGHs from O-Br
13-39 Sketch your predictions of the proton NMR spectra of the following compounds. (a) CH-0-CH.CH ~ NH₂ (b) (CH3),CH-C-CH CH; (1) CH-O CH (c) CI-CH2 - CH2 - CH2-a но NO₂ 0 H₂CCCC_CH₃ H 13-40 NH2 Tell precisely how you would nee the nton NMD
outline labratory syntheses of each of the following compounds starting with benzene and any other reagents Outline laboratory syntheses of each of the following compounds, starting with benzene and any other reagents. (c) CI (a) p-nitrotoluene (b) p-dibromobenzene (c) p-chloroacetophenone (d) m-nitrobenzenesulfonic acid (e) p-chloronitrobenzene (f) 1,3,5-trinitrobenzene (g) 2,6-dibromo-4-nitrotoluene
Propose a synthesis. Also this question have two separate photos Propose syntheses of the following compounds from cyclohexanone and any other necessary reagents. a. 2-butylcyclohexanone b. 2-butyl-6-methylcyclohexanone 2-butyl-2-methylcyclohexanone
3. Propose reasonable syntheses of each of the following compounds from the given starting materials. You may use any other readily available alkyl halides, solvents and reagents as necessary. More than one step is necessary. Show all intermediates, reactions, reagents and conditions clearly. It is not necessary to show the mechanism. HCECH HCECH , X HCECH HC=CH M H OHC (30 marks)
Question 2 Which of the following is the weakest base? NH, CH,NH HN- H N- - - 0 = 0 = 0 2 0 Question 3 How is N- classified? A a quarternary ammonium ion B a quarternary amine oc a secondary amine OD. a primary amine O E a tertiary amine Question 4 What would be the final organic product of the following reaction? NaCN CH.CH,CI - organic 1) excess LiAlH product 2) H0 . C6H5CH2CH2C02H OB C6H5CH2CH2NH2 CH,CH,CHCN...
Arrange the following compounds in order of increasing boiling point. A CH B CH.CH DCH (CH) H. .CH CH Н. H H H H CH H H H H H CH,CH) H CH.CH CH CH.CH Select) ve Select] [Select) [Select