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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Sand dunes would be created due to the mixture falling on each other
x
7. 1,2,2,2
8. 4,3,1
9. 1,4,1,2
10. 3,4,1,4
<u>Answer:</u> The correct answer is Option D.
<u>Explanation:</u>
We are given that car travels with a speed of 80 km/hr and we need to convert it into hm/s.
For that we use the conversions:
1 kilometer = 10 hectometer
And, 1 hour = 3600 seconds
To convert the quantity into hm/s, we multiply the numerator which is 80 by 10 to convert the whole quantity into hm/hr and now, to convert the result into hm/s finally, we divide the result by 3600.

Hence, the correct answer is option D.