Answer:
In order of decreasing miscibility
C₉H₂₀ (nonane)→C₂H₅F (fluoroethane)→C₂H₅Cl (chloroethane)→H₂O (water)
Explanation:
The solubility of a solid is a measure of its ability to dissolve in a liquid while for liquids, the miscibility is a measure of thhe liquid to mix with anoyjer liquid resulting in a soltion which can hold any amount of either liquids. Immiscible liquids are those that are not soluble or have very limited solibility with each other.
C₉H₂₀ (nonane)→C₂H₅F (fluoroethane)→C₂H₅Cl (chloroethane)→H₂O (water)
In the order of decreasing miscibility as like dissolve like, ability to dissociate and polar and organic characteristics are considered
Correct, Was that a question.
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.
Learn more about carbonyl here:
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Answer:
option "B" is correct (substance 2)
