D) During the nitration of benzene ring by conc. nitric acid in presence of conc. sulfuric...
D) During the nitration of benzene ring by conc. nitric acid in presence of conc. sulfuric acid, conc. nitric acid acts as:
E) Which of the following alcohol can't be oxidized even with stronger oxidizing agent as chromic acid?
Please explain, thank you!
Homework Answers
nitric acid accepts a proton from sulfuric acid and dissociates to form nitronium ion (NO2+) this nitronium ion acts as electrophile and nitrates the benzene ring.
tertiary alcohols can not be oxidized by strong oxidizing agents because there is no C-H bond in tert-alcohols.
Add Answer to:
D) During the nitration of benzene ring by conc. nitric acid in
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4. Consider the following unbalanced net redox equation: HCI + KMnO, (aq) + H,02 (aq) -. MnC12 (aq) + O2 (g) + KCI in an acid solution a. Determine the oxidation state of each atom or ion in the above reaction: b. Which atom is being oxidized? Which atom is being reduced? C. Which species is the reducing agent? Which is the oxidizing agent? d. Write the net...
Nitrobenzene is made by the direct nitration of benzene by nitric acid in the presence of strong sulphuric acid solution: CHe+HNOCH,NO2+H2O The actual nitrating agent is the nitronium ion, NO27, and the sulphuric acid is needed to generate this from the nitric acid feed Reconcentrated sulphuric acid, of strength 74% by weight and XC is mixed with pure nitric acid at 25°C to give a nitric acid strength in the mixture of 7.5% by weight. The heat of mixing causes...
Arrange the haloalkanes in
order of increasing reactivity in an Sn2 reaction with NaI in
acetone (least first).
a. Methyl bromide b Isopropyl chloride t-butyl iodide d. Isobutyl chloride aus CH3 cиз C. Arrange the haloalkanes in order of increasing reactivity in an SN2 reaction with Nal in acetone (least first). CH3 - CH2CH2-I C-Br CI Br CH3 I 11 II IV I, IV, III, II b II, II, I, IV a. IV,I, II, II с. d. III, II, IV,...
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Can
you please explain this? Thank you.
14) An L-aldohexose, X, is treated with nitric acid to yield optically inactive aldaric acid (a diacid). The same L-aldohexose is subjected to Ruff degradation and the degradation product is oxidized with nitric acid to produce another optically inactive aldaric acid. What is a possible structure of L-aldohexose X? он он он он НОЕНН-Нон нон нон н -он н -он нон но -н НЕОН нон но -н но-н но -н но -н но-н...
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please help solve question 23, question 24 and question 25.
thank you
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PLEASE ANSWER EACH QUESTION OR DO NOT ANSWER AT ALL. THANK
YOU!
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