Well it's an alkali metal if that's what you're asking<span />
Answer: 250 ml of stock solution with molarity of 12.0 M is measured using a pipette and 250 ml of water is added to volumetric flask of 500 ml to make the final volume of 500 ml.
Explanation:
According to the dilution law,
where,
= concentration of stock solution = 12.0 M
= volume of stock solution = ?
= concentration of diluted solution= 6.00 M
= volume of diluted acid solution = 500 ml
Putting in the values we get:
Thus 250 ml of stock solution with molarity of 12.0 M is measured using a pipette and 250 ml of water is added to volumetric flask of 500 ml to make the final volume of 500 ml.
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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Solid liquid and gas is the answer