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:
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Its going to b 5,800,000 due to each Km being 1,000,000 Mm
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We use prefixes in ionic compounds Don't use numeric prefixes like mono, di, tri, etc. when naming ionic compounds - they are used only to denote covalent molecular compounds.
Answer:
Specific heat of ethyl chloride in gas and liquid phases, enthalpy of vaporization and specific heat of solid surface.
Explanation:
In order to determine the final temperature, the heat lost by the chloride needs to be found. This would require the specific heat in both phases and the enthalpy of vaporization. (you will use q=mc(delta)T and q=m(delta)H)
Then the energy gained by the surface needs to be found. This will require the specific heat in order to use the q=mc(delta)T equation.