7. Compound EE, C4H3O shows a positive result (formation of yellow precipitate) when reacted with lodoform reagent. Reduction of compound EE with sodium boron hydride, NABH4 followed by acidified water, H3O* produces an alcohol FF. Compound FF is treated with phosporus pentachloride, PCI5 to form compound GG. Prolong heating of compound EE with concentrated solution of acidified potassium permanganate, KMNO4 will form compound HH and II. Sebatian EE, C4H%O menunjukkan keputusan positif (pembentukkan mendakan kuning) apabila bertindak balas dengan reagen lodoform. Penurunan sebatian EE dengan natrium boron hidrida, NABH4 diikuti dengan air berasid, H3O* menghasilkan satu alkohol FF. Sebatian FF telah dirawat dengan fosforus pentaklorida, PCI5 untuk membentuk sebatian GG. Pemanasan yang berterusan bagi sebatian EE dengan larutan pekat kalium permanganat, KMNO4 berasid akan membentuk sebatian HH dan II. Draw the structural formula of EE, FF, GG, HH and II. Lukiskan formula struktur bagi EE, FF, GG, HH and II.

7. Compound EE, C4H3O shows a positive result (formation of yellow precipitate) when reacted with lodoform reagent. Reduction of compound EE with sodium boron hydride, NABH4 followed by acidified water, H3O* produces an alcohol FF. Compound FF is treated with phosporus pentachloride, PCI5 to form compound GG. Prolong heating of compound EE with concentrated solution of acidified potassium permanganate, KMNO4 will form compound HH and II. Sebatian EE, C4H%O menunjukkan keputusan positif (pembentukkan mendakan kuning) apabila bertindak balas dengan reagen lodoform. Penurunan sebatian EE dengan natrium boron hidrida, NABH4 diikuti dengan air berasid, H3O* menghasilkan satu alkohol FF. Sebatian FF telah dirawat dengan fosforus pentaklorida, PCI5 untuk membentuk sebatian GG. Pemanasan yang berterusan bagi sebatian EE dengan larutan pekat kalium permanganat, KMNO4 berasid akan membentuk sebatian HH dan II. Draw the structural formula of EE, FF, GG, HH and II. Lukiskan formula struktur bagi EE, FF, GG, HH and II.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

You are given a mixture of benzoic acid, 2-naphthol and 1,4-dimethoxybenzene and you are asked to separate the mixture into its following compounds. You are limited to using dichloromethane, pentane, cyclohexane and ethyl acetate as organic solvents. This doesn't involve solvents used to convert the 3 compounds to ionic salts. Suggest possible organic solvents and explain a procedure you would carry out to separate the 3 mixtures briefly.
What compound is formed when a dilute solution of cyclohexanone is shaken with NaOD in D2O for several hours?
Describe the process (Step by Step) of the fractional distillation of 4-t-butylcyclohexanol and 4-t-butylcyclohexene
Isoerythrogenic acid, C18H26O2, is an acetylic fatty acid that turns a vivid blue on exposure to UV light. On Catalytic hydrogenation over a palladium catalyst, five molar equivalents of hydrogen are absorbed, and stearic acid, CH3(CH2)16CO2H, is produced. Ozonolysis of isoerythrogenic acid yields the following products: formaldehyde, CH2O, malonic acid, HO2CCH2CO2H, adipic acid, HO2C(CH2)4CO2H, and the aldehyde carboxylic acid, OHC(CH2)6CO2H. Provide a structure for isoerythrogenic acid.
08) The NMR spectra of the two isomeric compounds with formula C3H5ClO2 are shown in letters a and b. Low-field protons appearing in the NMR spectrum around 12.1 and 11.5 ppm, respectively, are shown highlighted. Draw the structures of the isomers.
1. Provide the reagents necessary to carry out the following conversion. ملا علی H
Obtain 3-chloro-4-nitrophenol by starting from benzene and by diazotization using suitable reagents.
5B Using benzene as a raw material and reagents of your choice, propose a method of preparing 4-ethylaniline
Compound EE, C4H8O shows a positive result (formation of yellow precipitate) when reacted with lodoform reagent. Reduction of compound EE with sodium boron hydride, NABH4 followed by acidified water, H3O* produces an alcohol FF. Compound FF is treated with phosporus pentachloride, PCI5 to form compound GG. Prolong heating of compound EE with concentrated solution of acidified potassium permanganate, KMNO4 will form compound HH and II. Sebatian EE, C4H8O menunjukkan keputusan positif (pembentukkan mendakan kuning) apabila bertindak balas dengan reagen lodoform. Penurunan sebatian EE dengan natrium boron hidrida, NaBH4 diikuti dengan air berasid, H30* menghasilkan satu alkohol FF. Sebatian FF telah dirawat dengan fosforus pentaklorida, PCI5 untuk membentuk sebatian GG. Pemanasan yang berterusan bagi sebatian EE dengan larutan pekat kalium permanganat, KMNO4 berasid akan membentuk sebatian HH dan II. Draw the structural formula of EE, FF, GG, HH and II. Lukiskan formula struktur bagi EE,…
Define what is reduction reaction, reducing agents, weak and strong reducing agents sodium borohydride reduction with benzophenone and sodium borohyride to get benzophenone
Name the following compounds A and B. How could you distinguish these two molecules by using 1H NMR and IR techniques? Propose an analytical technique to determine the iron content of these compounds. Calculate the mass percentages of C and H of compound B (C: 12.01 g/mol; H: 1.008 g/mol; Fe: 55.845 g/mol).
7. Compound AA, C4H®O, gives a positive result (formation of a silver mirror) when reacted with Tollen's reagent. Reduction of compound AA with lithium aluminium hydride, LİAIH4 followed by acidified water, H3O* produces an alcohol, BB. Oxidation of BB with hot acidified potassium dichromate, K2Cr207 gives butanoic acid, C3H7COOH. Esterification between butanoic acid and methanol, CH3OH produces compound CC. Dehydration of compound BB using concentrated sulphuric acid, H2SO4 at a temperature of 180°C produces compound DD.