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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The correct answer is option 1. Carbon dioxide is nonpolar because the shape of the molecule is symmetrical. It is a linear molecule where the oxygen atoms are symmetrical on each end. CO2 molecule do not have a region of unequal sharing.
Answer:
This is a typical stoichiometry question.To answer this question you want to get a relationship between
N
a
2
O and NaOH.
So you can get a relationship between the moles of
N
a
2
O
and moles of NaOH by the concept of stoichiometry.
N
a
2
O +
H
2
O ----------------> 2 NaOH.
According to above balanced equation we can have the stoichiometry relationship between
N
a
2
O and NaOH. as 1:2
It means 1 moles of
N
a
2
O is required to react with one mol of
H
2
O to produce 2 moles of NaOH.
in terms of mass 1 mole of
N
a
2
O has mass 62 g on reaction with water produces 2 moles of NaOH or 80 g of NaOH.
62 g of
N
a
2
O produces 80 g of NaOH.
1g of NaOH is produced from 62/80 g of
N
a
2
O
1.6 x
10
2
g of NaOH will require 62 x 1.6 x
10
2
g / 80 of
N
a
2
O
124g of
N
a
2
O.
Explanation:
