Explanation:
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It is a poly atomic anion because it has more than one atom and a negative charge
Resonance, leaving group, carbonyl carbon delta+, and steric effect is the most crucial variables that affect the relative reactivity of a functional group containing a carbonyl in an addition or substitution process.
Discussion:
1. Carbonyl Carbon Delta+: The carbonyl group becomes more electrophilic and accelerates nucleophilic assault when the carbonyl carbon delta+ is bigger.
2. Resonance: When the carbonyl is transformed into the tetrahedral adduct, it may be lost. Loss of resonance increases the energy of the transition state for this nucleophilic assault because resonance has the function of stabilizing. Therefore, a carbonyl functional group's resistance to nucleophilic attack increases as resonance in the group increases in importance.
3. Leaving group: Tetrahedral adduct fragmentation is encouraged by a better LG.
4. Steric effects: The nucleophilic attack on carbonyl carbon is delayed when sterically impeded.
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Alchemists advanced the tools and procedures for working with chemicals. Alchemists also developed methods for sorting out mixtures and cleansing chemicals. They designed equipment that is still in use today including beakers, flasks, tongs, funnels, and the mortar and pestle. Also, Alchemists backed to an unbelievable variety of what would later be acquainted as chemical industries: basic metallurgy, metalworking, the invention of inks, dyes, paints, and cosmetics, leather-tanning, and the preparation of extracts and liquors.
Because it requires lots of electricity to turn it into an aqueous solution so that electrolysis can be performed on it.
