Why? Isn't a strong base/oxidizing agent needed to deprotonate an alcohol?
Correct answer is B. Here is your explanation.
Why? Isn't a strong base/oxidizing agent needed to deprotonate an alcohol?
Write a balanced REDOX equation between a strong elemental reducing agent and a strong elemental oxidizing agent.
24) The hypochlorite ion (OCl-) is a strong oxidizing agent often found in household bleaches and disinfectants. It is also the active ingredient that forms when swimming pool water is treated with chlorine. In addition to its oxidizing abilities, the hypochlorite ion has a relatively high affinity for protons (it is a much stronger base than Cl-, for example) and forms the weakly acidic hypochlorous acid (HOCl, Ka = 3.5 x 10-8). Calculate the pH of a 0.100 M aqueous...
The hypochlorite ion (OCl-) is a strong oxidizing agent often found in household bleaches and disinfectants. It is also the active ingredient that forms when swimming pool water is treated with chlorine. In addition to its oxidizing abilities, the hypochlorite ion has a relatively high affinity for protons (it is a much stronger base than Cl-, for example) and forms the weakly acidic hypochlorous acid (HOCl, Ka = 3.5 x 10-8). Calculate the pH of a 0.100 M aqueous solution...
Why is K2S2O8 such a powerful oxidizing agent?
3. Write an equation for the oxidation of each alcohol below. Indicate the oxidizing agent on the arrow. If no reaction occurs, write "no reaction" after the arrow (a) CH.CH.CH.CH.CH OH (b) CH CHCCH.CH OH (c) CH.CHCH.CH.CH.CH OH
Question 4 The base used to deprotonate diethyl malonate is always ethoxide. The base should be the same as the leaving group on the ester. What would happen if hydroxide was used instead? O Nothing, hydroxide is not a strong enough base to deprotonate diethyl malonate O Hydroxide could also act as a nucleophile and do a saponification reaction on the ester O The decarboxylation step would not work with hydroxide Question 5
Why is nitric acid a stronger oxidizing agent than sodium dichromate? I am oxidizing from an organic compound (cyclohexanol).
of CHICH CH2OH with an oxidizing agent will prodace 2 Treatmens A) an aldehyde iting B) a ketone D) a thiol E) no reaction tof CH CH2OH with an oxidizing agent will produce 21. Treatment teacher give A) an aldehyde B) acetaldehyde t legibie C) acetic acid D) a carboxylic acid E) all of the above are understood to be true by the organic chemist guote or P 22. Oxidation of a secondary alcohol will produce A) an aldehyde B)...
*PLEASE ANSWER CORRECTLY IT'S FOR A TEST* Alcohol Reactions QUESTION ANSWER SOCl2 Which oxidizing agent is best for the following reaction: Jones Reagent оооо HO он NaOCI (Bleach) PCC
Identify the oxidizing agent and the reducing agent on the reactant side of the following chemical equation. Then explain why you selected these compounds as the oxidizing agent and the reducing agent. MnO4 (aq) + SO2(aq) → MnO2(s) + 5042 (aq)