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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8.3mL
Explanation:
Given parameters:
Mass of acetone = 6.54g
Density of acetone = 0.7857 g/mL
Unknown:
Volume of acetone = ?
Solution:
Density is defined as the mass per unit volume of a substance. It is expressed mathematically as shown below:
Density = 
Since the unknown is volume, we make it the subject of the formula
Volume = 
Input the values;
Volume = 
= 8.3mL
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Salinity has units of grams NaCl or salt per kilogram solution. We can use the density given and the molar mass of the salt to convert from salinity to molarity. We do as follows:
( 5.6 g / kg ) ( 1.03 kg / L ) ( 1 mol / 58.44 g ) = 0.0987 mol NaCl / L
Explanation:
As a substance melts, and goes from a solid to a liquid state, the kinetic energy of the molecules increases, and the molecules move faster, and they separate further and further away from each other. The intermolecluar forces holding the molecules together become weaker
