Answer:
Option C, (Actual yield ÷ percent yield) × 100
Explanation:
Theoretical yield is defined as the total amount of product formed for given reactants in a chemical reaction. It is an ideal case which assumes no exceptions or wastage.
The mathematical relation between the actual yield, percent yield and theoretical yield is as follows -
Where
P.Y. represents the percent yield a
M A.Y. represents the mass obtained from actual yield
M T.Y. represents the mass obtained from theoretical yield
Hence, if we rearrange the formula, we get -
Hence, option C is correct
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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Not sure but it might be A or B
