Answer:
3.5 atm
Explanation:
As stated in the question pressure is required to counteract the natural tendency for water to dilute the more concentrated solution. The difference in concentrations will give us the answer using the osmotic pressure equation.
π = ( n/v) RT where n/v is the molarity (mol/L), R is the gas constant and T is the temperature.
The difference in osmotic pressure of the solutions is:
Δπ = Δ c RT where c is the difference in molar concentrations.
pressure required = Δπ = (0.190 - 0.048) M x 0.821 Latm/Kmol x 298 K
= 3.47 atm
Answer:
-5.51 kJ/mol
Explanation:
Step 1: Calculate the heat required to heat the water.
We use the following expression.

where,
- c: specific heat capacity
- m: mass
- ΔT: change in the temperature
The average density of water is 1 g/mL, so 75.0 mL ≅ 75.0 g.

Step 2: Calculate the heat released by the methane
According to the law of conservation of energy, the sum of the heat released by the combustion of methane (Qc) and the heat absorbed by the water (Qw) is zero
Qc + Qw = 0
Qc = -Qw = -22.0 kJ
Step 3: Calculate the molar heat of combustion of methane.
The molar mass of methane is 16.04 g/mol. We use this data to find the molar heat of combustion of methane, considering that 22.0 kJ are released by the combustion of 64.00 g of methane.

Answer:
Let's say we were Subtracting 3-2=? To Find the Answer we would Subtract 2 from 3 which is 1 Simple our answer is 1 But let's say the Question is 3 - 1= ? to find this answer we would subtract 1 from 3 which is 2 Let's say you were subtracting 3-3=? to do this we take 3 away from 3 now 3 is 0 so our answer is 0 so there are 3 different problems we can make with 3 we could make more but I'm just telling the basics Hope I Helped Bye :)
Explanation:
Carbon-12 has the following electron configuration: 1s2-2s2-2p2. As seen in the configuration, the right answer is: the first electron shell has 4 orbitals.
Answer:
See explanation
Explanation:
A. Constitutional or structural isomers have the same molecular formula but different structural formulas.
B. Conformational isomers are compounds having the same atom to atom connectivity but differ by rotation about one or more single bonds.
C. Stereo isomers are compounds having the same molecular mass and atom to atom connectivity but different arrangement of atoms and groups in space.
I. Enantiomers are stereo isomers (optical isomers particularly) that are non-superimposable mirror images of each other.
II. Diasteromers are optical isomers that are not mirror images of each other.
Both diasteromers and enantiomers are types of optical isomers which in turn is one of the types of stereo isomers.
Stereo isomers differ from conformational isomers in that the arrangement of atoms in stereo isomers is permanent while conformational isomers results from free rotations in molecules about single bonds.