Answer:
The reactive nucleophile is Ketone.
Explanation:
In organic chemistry, The process of acid - catalyzed aldol condensation starts from when ketone (or any aldehyde) is converted to an -enol, after which it attacks another ketone/aldehyde that has already been activated by parbonyl oxygen protonation.
The process of this is that first of all the ketone undergoes tautomerization to form -enol. Thereafter, the other carbonyl will undergo protonation which makes the carbon activated towards attack. Now, the nucleophilic enol will be added to the carbonyl in a [1,2]-addition reaction and we will now use deprotonation to obtain the neutral Aldol product.
Now, since only the ketone can produce an -enol, thus it is the nucleophile as aldehydes are better electrophiles
The false positive from the response of hydrogen peroxide and the immunizing circle would be created by poor specificity. The recipe for specificity is TN/TN+FP. False-positive outcomes can be ascribed to meddling substances in nature where the strips are put away or utilized, for example, hydrogen peroxide (H2O2) or fade (hypochlorite).
Answer: D i think
Explanation: Im sorry if it is wrong lol!! I pretty sure thats the answer...
Answer: C. HNO3 and NaOH
Explanation:
Arrhenius acid produces hydogen ion (H+) when dissolved in water. An example of Arrhenius acid is HNO3.
Arrhenius base produces hydroxyl ion (OH-) when dissolved water. An example of Arrhenius base is NaOH.
