D milk turning sour
the other options are physical changes
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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At STP one mol weighs 22.4L
Moles of O_2
1 mol.O_2 can create 2mol water
moles of water
Volume of water
<u>Answer:</u> Carbon-carbon double bond is stronger and shorter than the single bond.
<u>Explanation:</u>
It is given that carbon-carbon double bond has greater energy than the carbon-carbon single bond.
Bond energy is directly proportional to the bond strength, which means that the double bond will have greater strength than single bond and triple bond has the greatest strength of all the bonds.

Bond energy is inversely proportional to the bond length of the carbon-carbon bond. This means that more is the bond energy, shorter will be the bond and vice-versa.

Hence, carbon-carbon double bond is stronger and shorter than the single bond.