Answer:
Option (A)
Explanation:
The dew point refers to the temperature at which the amount of water vapor present in the air is so high that the relative humidity becomes 100%, and with the increasing rate of cooling, the condensation process takes place and dew is formed.
So for dew point to occur, the air temperature must reach a condition where the air is fully saturated or the relative humidity is 100%.
Thus, the correct answer is option (A).
Explanation:
Adhesion means the ability to stick on the surface of another substance.
Water exhibits adhesive forces due to which it is able to stick to the glass. Due to adhesive forces water spreads over the surface of glass and sticks to it.
These adhesive forces between the glass and water enough that it deforms the spherical shape of water molecules and help them stick to the surface of glass. As a result, adhesive forces overcome the repulsion between like molecules.
Hence, water is able to “stick” to the side of glass due to strong adhesive forces.
Answer:
47.36mL
Explanation:
Using Boyles law equation, which states that:
P1V1 = P2V2
Where;
V1 = initial volume (mL)
V2 = final volume (mL)
P1 = initial pressure (atm)
P2 = final pressure (atm)
Based on the provided information, V1 = 25.3mL, P1 = 152 kPa, V2 = ?, P2 = 0.804atm
First, we need to convert 152kPa to atm by dividing by 101
1kPa = 0.0099atm
152kPa = 1.505atm
P1V1 = P2V2
1.505 × 25.3 = 0.804 × V2
38.08 = 0.804V2
V2 = 38.08/0.804
V2 = 47.36mL
Answer: 6.75 moles
Explanation:
This is a simple stoichiometry proboe. that I would set up like this:
(13.5 moles CuCI2) (1 mol I2 / 2 moles CuCi2)
That means you all you have to do for this problem is divide by 2 and cancel out the unit moles CuCI2, which leaves you with 6.75 moles I2.
Hope this helps :)
Answer:
See detailed mechanism in the image attached
Explanation:
The mechanism shown in detail below is the synthesis of serine in steps.
The first step is the attack of the ethoxide ion base on the diethyl acetamidomalonate substrate giving the enolate and formaldehyde.
The second step is the protonation of the oxyanion from (1) above to form an alcohol as shown.
Acid hydrolysis of the alcohol formed in (3) above yields a tetrahedral intermediate, a dicarboxyamino alcohol.
Decarboxylation of this dicarboxyamino alcohol yields serine, the final product as shown in the image attached.