Yes, you should memorize them. While it is easy to predict them by looking at a periodic table, you should still have a strong grasp of simpler chemistry such as this before more challenging topics are taught.
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Acetone has α-hydrogens (on both sides) and thus can be deprotonated to give a nucleophilic enolate anion. The aldehyde carbonyl is much more electrophilic than that of a ketone, and therefore reacts rapidly with the enolate.
<h3>What is nitrobenzaldehyde?</h3>
- Synthesis. The synthesis of 3-nitrobenzaldehyde is achieved via nitration of benzaldehyde, which yields especially the meta-isomer. Creation allocation is about 19% for the ortho-, 72% for the meta- and 9% for the para isomers.
- Acetone, propanone, or dimethyl ketone, is an organic combination with the formula (CH3)2CO. It is the easiest and smallest ketone. It is a colorless, highly volatile, and combustible liquid with a characteristic aromatic odor.
- Nitration of benzene with conc nitric acid and conc sulphuric acid gives nitrobenzene. Chlorination with chlorine in the existence of anhydrous aluminum chloride gives meta nitro chlorobenzene.
To learn more about sulphuric acid, refer to:
brainly.com/question/4018599
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Answer:
Your correct answer is D. 40 g
Explanation:
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