<h3>
Answer:</h3>
915 Joules
<h3>
Explanation:</h3>
- The heat of fusion is the heat that is required to convert a given mass of a substance from solid state to liquid state without change in temperature.
- In this case, we are given specific heat of a substance as 122 joules per gram
- It means that amount of heat equivalent to 122 joules is required to change 1 gram of the substance from solid state to liquid state.
- Therefore, we can determine the amount of heat needed to change 7.5 grams of the substance from solid to liquid state.
1 g = 122 Joules
7.5 g = ?
= 122 × 7.5
= 915 Joules
Thus, 7.5 g of the substance at its melting point will require 915 Joules of heat to melt.
<span>Because mona means 1 atom, and a compound is made up of 2 or more atoms.</span>
Answer:
A
Explanation:
CH4+O2-CO2+ H20
that mean methane has burn in oxygen to produce CO2
A sample of an ideal gas has a volume of 2.30 L at 281 K and 1.02 atm. 1.76 atm is the pressure when the volume is 1.41 L and the temperature is 298 K.
<h3>What is Combined Gas Law ?</h3>
This law combined the three gas laws that is (i) Charle's Law (ii) Gay-Lussac's Law and (iii) Boyle's law.
It is expressed as
where,
P₁ = first pressure
P₂ = second pressure
V₁ = first volume
V₂ = second volume
T₁ = first temperature
T₂ = second temperature
Now put the values in above expression we get
P₂ = 1.76 atm
Thus from the above conclusion we can say that A sample of an ideal gas has a volume of 2.30 L at 281 K and 1.02 atm. 1.76 atm is the pressure when the volume is 1.41 L and the temperature is 298 K.
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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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