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If you wanted to harvest cranberries you would need to use flotation.
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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
<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.