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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A. thermal energy
like when the computer gets hot after running for so long
Answer:
4 moles of carbon
6 moles of water
Explanation:
I think as there no data given u have to is the numbers infront of the equation e.g 4CO2 so 4.
hope this helps :)
Answer:
No
Explanation:
The mass fraction is defined as:
where:
- wi: mass fraction of the substance i
- mi: mass of the substance i
- mt: total mass of the system
<u><em>The mass fraction of two substances (A and B), will be the same, ONLY if the mass of the substance A (mA) is the same as the mass of the substance B (mB).</em></u>
An equimolar mixutre of O2 and N2 has the same amount of moles of oxygen and nitrogen, just to give an example let's say that the system has 1 mole of O2 and 1 mole of N2. Then using the molecuar weigth of each of them we can calculate the mass:
mA= 1 mole of O2 * 16 g/1mol = 16 g
mB=1 mole of N2 *28 g/1mol=28 g
As mA≠mB then the mass fractions are not equal, so the answear is NO.
