Answer:
A. standing in line to pay for groceries.
Explanation:
Just standing there is not doing work, All of the other options are examples of work.
<span>the water is the solvent, and the powder is the solute. This is also a solution altogether. </span>
Twice as much more will the freezing point of water be lowered in beaker a than in beaker b.
<h3>What determines freezing point?</h3>
A liquid's freezing point rises if the intermolecular interactions between its molecules are strong. The freezing point, however, drops if the molecules of inter - molecular are minimal. The process through which a substance transforms from a liquid into a solid is known as freezing.
<h3>How significant is freezing point?</h3>
Freezing points play a big role in occupational safety. A chemical may perhaps turn harmful if held below its freezing point. A critical safety benchmark for assessing the effects of worker exposure to cold environments is the freezing point.
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Answer:
Yes, it is possible.
Explanation:
A diprotic acid is an acid that can release two protons. That's why it is called diprotic.
Monoprotic → Release one proton, for example Formic acid HCOOH
Triprotic → Releases three protons, for example H₃PO₄
Polyprotic → Release many protons, for example EDTA
it is a weak acid.
In the first equilibrum, it release proton, and the second is released in the second equilibrium. So the first equilibrium will have a Ka1
H₂A + H₂O ⇄ H₃O⁺ + HA⁻ Ka₁
HA⁻ + H₂O ⇄ H₃O⁺ + A⁻² Ka₂
The HA⁻ will work as an amphoterous because, it can be a base or an acid, according to this:
HA⁻ + H₂O ⇄ H₃O⁺ + A⁻² Ka₂
HA⁻ + H₂O ⇄ OH⁻ + H₂A Kb₂
Conjugated dienes routinely undergo 1,2 and 1,4 addition reactions with a variety of electrophilic reagents; this suggests that electrophilic reagents are likely intermediates during these reactions.
Two double bonds and one single bond divide a conjugated diene into two halves. Nonconjugated (Isolated) Dienes have more than one single bond separating two double bonds. Two double bonds are joined to the same atom to form cumulated dienes.
Reagents that function by acquiring electrons or sharing electrons that once belonged to a foreign molecule are referred to as electrophilic reagents, or electrophiles, in some cases. Electrophiles are molecules with a positive charge and a lack of electrons that can react by exchanging electron pairs with nucleophiles, which have many electrons. Epoxides, hydroxy amines, nitroso and azoxy derivatives, nitrenium ions, and elemental sulfur are significant electrophiles.
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