Answer:
The type of collision is A. Inelastic collision.
Explanation:
The macroscopic collisions are generally inelastic and do not conserve the kinetic energy, although of course the total energy is conserved. The inelastic collision is one in which the objects that collide remain together after the collision.
So, a figure skater skating across ice, who grabs another skater and brings him along the ice with her is a clear example of inelastic collision.
Explanation:
Medieval number one. There you havt it.
Answer:
Explanation:
<u>1) Data:</u>
a) V = 93.90 ml
b) T = 28°C
c) P₁ = 744 mmHg
d) P₂ = 28.25 mmHg
d) n = ?
<u>2) Conversion of units</u>
a) V = 93.90 ml × 1.000 liter / 1,000 ml = 0.09390 liter
b) T = 28°C = 28 + 273.15 K = 301.15 K
c) P₁ = 744 mmHg × 1 atm / 760 mmHg = 0.9789 atm
d) P₂ = 28.5 mmHg × 1 atm / 760 mmHg = 0.0375 atm
<u>3) Chemical principles and formulae</u>
a) The total pressure of a mixture of gases is equal to the sum of the partial pressures of each gas. Hence, the partical pressure of the hydrogen gas collected is equal to the total pressure less the vapor pressure of water.
b) Ideal gas equation: pV = nRT
<u>4) Solution:</u>
a) Partial pressure of hydrogen gas: 0.9789 atm - 0.0375 atm = 0.9414 atm
b) Moles of hygrogen gas:
pV = nRT ⇒ n = pV / (RT) =
n = (0.9414 atm × 0.09390 liter) / (0.0821 atm-liter /K-mol × 301.15K) =
n = 0.00358 mol (which is rounded to 3 significant figures) ← answer
I believe it is 65.37.
Let me know if this is correct. Also good luck!!
Benzaldehyde or C6H5CHO would not undergo the aldol condensation because it does not contain an alpha-hydrogen in its structure. Aldol condensation is a type of reaction that happens between an enolate and an aldehyde or ketone leading to a alkene that has a planar structure. The lack of an alpha-hydrogen would not allow for it to undergo such process since it cannot enolize. Benzaldehyde undergoes a nucleophilic reaction known as Claisen-Schmidt condensation. It has somehow same mechanism of the aldol reaction however, the nucleophilic attack on the carbonyl happens even without the alpha-hydrogen but with an enolate that is from a ketone.
