So I’m not 100% sure what you’re asking but I’m going to give it a go. The elimination reaction is a term used in organic chemistry that describes a type of reactions. The name kinda tells you what’s going to happen. Something is going to be removed/eliminated from initial reactant/substrate and as a result, an alkene (double bond containing compound) will form.
In elimination reactions a hydrogen atom is first removed (as a H+) from the beta carbon. As a result, the left behind electrons create a pi bond between the beta carbon and the neighboring alpha carbon. This promotes the electronegative atom, on the alpha carbon, to leaves the substrate taking both electrons from the shared sigma bond with the alpha carbon.
Psolution = X · PH_20
= 0.966 · 31.8 torr
= 30.7 torr
The element name is: Antimony
The chemical symbol: Sb
Atomic Mass: 121.75
Atomic Number: 51
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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