Answer:
Shape- square planar , hybridisation-sp3
Explanation:
Shape:
- VSPER theorey is used to determine both electron geometry and molecular geometry of a molecule.(PtCl4)2 molecular geometry is square planar
- Hybridisation:It undergoes sp3 hybridisation.since there are 2 unpaired electrons in this case, it is paramagnetic in nature
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The prefix milli means thousand so the correct conversion factor is 1000mg/g
Answer:
Explanation:
To calculate the cell potential we use the relation:
Eº cell = Eº oxidation + Eº reduction
Now in order to determine which of the species is going to be oxidized, we have to remember that the more the value of the reduction potential is negative, the greater its tendency to be oxidized is. In electrochemistry we use the values of the reductions potential in the tables for simplicity because the only thing we need to do is change the sign of the reduction potential for the oxized species .
So the species that is going to be oxidized is the Aluminium, and therefore:
Eº cell = -( -1.66 V ) + 0.340 V = 5.06 V
Equally valid is to write the equation as:
Eº cell = Eº reduction for the reduced species - Eº reduction for the oxidized species
These two expressions are equivalent, choose the one you fell more comfortable but be careful with the signs.
Answer:
C. Lose three electrons to have a full outer shell
Explanation:
Al is in Group 13 of the Periodic Table, so it has three valence electrons.
It must either lose three electrons or gain five to achieve a stable octet.
It is easier to lose three electrons than it is to gain five, so Al loses three electrons.
D. is wrong, for the same reason.
A. is wrong. If Al lost three electrons, it would be breaking into a stable inner shell.
C. is wrong. Al is a metal, so it will lose electrons in a reaction.
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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