It is a constant-volume type calorimeter that measures the heat of a particular reaction or measures the calorific value of the fuels. Bomb calorimeters are built in such a way that they can withstand the large pressure produced within the calorimeter due to the reaction or burning of fuel.
It can be done. Normally the boiling point of water is 100°C. It will boil at temperature greater than 100°C more quickly. Water can be boiled at 95°C but for that the atmospheric pressure of the water should be decreased which will decrease the boiling point of water.
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To boil water at 95°C, decrease the atmospheric pressure.
At 105°C, the water will be boiling quickly than normal at 100°C.
Answer:
When nitric acid combine with sodium hydroxide the salt formed is called sodium nitrate. option B
Explanation:
It is the strong acid strong base reaction. When acid and base react with each other salt and water are formed.
In given reaction nitric acid combine with sodium hydroxide base and form sodium nitrate salt and water.
Chemical equation:
HNO₃(aq) + NaOH(aq) → NaNO₃(aq) + H₂O(l)
Ionic equation:
H⁺NO₃⁻(aq) + Na⁺OH⁻(aq) → Na⁺NO₃⁻(aq) + H₂O(l)
Net ionic equation:
H⁺(aq) + OH⁻(aq) → H₂O(l)
The Na⁺(aq) and NO₃⁻(aq) are spectator ions that's why these are not written in net ionic equation. The water can not be splitted into ions because it is present in liquid form.
Spectator ions:
These ions are same in both side of chemical reaction. These ions are cancel out. Their presence can not effect the equilibrium of reaction that's why these ions are omitted in net ionic equation.
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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