Mg(NO3)2 => <span>Magnesium nitrate
hope this helps!</span>
Answer:
a) Xbenzene = 0.283
b) Xtoluene = 0.717
Explanation:
At T = 20°C:
⇒ vapor pressure of benzene (P*b) = 75 torr
⇒ vapor pressure toluene (P*t) = 22 torr
Raoult's law:
∴ Pi: partial pressure of i
∴ Xi: mole fraction
∴ P*i: vapor pressure at T
a) solution: benzene (b) + toluene (t)
∴ Psln = 37 torr; at T=20°C
⇒ Psln = Pb + Pt
∴ Pb = (Xb)*(P*b)
∴ Pt = (Xt)*(P*t)
∴ Xb + Xt = 1
⇒ Psln = 37 torr = (Xb)(75 torr) + (1 - Xb)(22 torr)
⇒ 37 torr - 22 torr = (75 torr)Xb - (22 torr)Xb
⇒ 15 torr = 53 torrXb
⇒ Xb = 15 torr / 53 torr
⇒ Xb = 0.283
b) Xb + Xt = 1
⇒ Xt = 1 - Xb
⇒ Xt = 1 - 0.283
⇒ Xt = 0.717
A. High intermolecular forces of attraction. If there are high intermolecular forces, the molecules will need large energies to escape into the liquid. The substance will nave a high melting point.
The other options are <em>incorrect </em>because they are <em>weak force</em>s. They would cause <em>low melting points</em>.
Answer:
Types of Potential Energy
Elastic Potential Energy. Anything that can act like a spring or a rubber band can have elastic potential energy. ...
Gravitational Potential Energy. There is a constant attractive force between the Earth and everything surrounding it, due to gravity. ...
Chemical Potential Energy.
(IF THIS HELPED CAN YOU GIVE ME A BRAINYLEST PLEASE?)
Answer : Option 1) The true statement is each carbon-oxygen bond is somewhere between a single and double bond and the actual structure of format is an average of the two resonance forms.
Explanation : The actual structure of formate is found to be a resonance hybrid of the two resonating forms. The actual structure for formate do not switches back and forth between two resonance forms.
The O atom in the formate molecule with one bond and three lone pairs, in the resonance form left with reference to the attached image, gets changed into O atom with two bonds and two lone pairs.
Again, the O atom with two bonds and two lone pairs on the resonance form left, changed into O atom with one bond and three lone pairs. It concludes that each carbon-oxygen bond is neither a single bond nor a double bond; each carbon-oxygen bond is somewhere between a single and double bond.
Also, it is seen that each oxygen atom does not have neither a double bond nor a single bond 50% of the time.
