Answer:
Heat or Thermal energy, Solar Energy, Chemical energy, electrical energy, mechanical energy
Explanation:
Explanation:
1 literThe total of water is equal to 1000.0 g of water
we need to find the molality of a solution containing 10.0 g of dissolved in Na₂S0₄1000.0 g of water
1. For that find the molar mass
Na: 2 x 22.99= 45.98
S: 32.07
O: 4 x 16= 64
The total molar mass is 142.05
We have to find the number of moles, y
To find the number of moles divide 10.0g by 142.05 g/mol.
So the number of moles is 0.0704 moles.
For the molarity, you need the number of moles divided by the volume. So, 0.0704 mol/1 L.
The molarity would end up being 0.0704 M
The molality of a solution containing 10.0 g of Na2SO4 dissolved in 1000.0 g of water is 0.0704 Mliter
Answer: 68
Explanation:
Isotopes of an element have same number of protons but different number of neutrons. Which means isotopes of an element have same atomic number but different mass number.
Atomic number is equal to the number of protons or the number of electrons for a neutral atom and is specific to a particular element.
Mass number is the sum of number of protons and the number of neutrons.
Given : atomic number of element Q = 68 = number of protons
Mass number of isotope Q-136 = 136
But as isotopes have same atomic number, the number of protons will be same and hence there are 68 protons are in a neutral atom of this isotope.
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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