Answer:
XCH₄ = 0.461
XCO₂ = 0.539
Explanation:
Step 1: Given data
- Partial pressure of methane (pCH₄): 431 mmHg
- Partial pressure of carbon dioxide (pCO₂): 504 mmHg
Step 2: Calculate the total pressure in the container
We will sum both partial pressures.
P = pCH₄ + pCO₂
P = 431 mmHg + 504 mmHg = 935 mmHg
Step 3: Calculate the mole fraction of each gas
We will use the following expression.
Xi = pi / P
XCH₄ = pCH₄/P = 431 mmHg/935 mmHg = 0.461
XCO₂ = pCO₂/P = 504 mmHg/935 mmHg = 0.539
 
        
             
        
        
        
I think B. As an idea is just a way that could be possible
        
             
        
        
        
The heat cause 300g water temperature increase from 20 to 26 celcius. The heat transferred would be: 300g * (26 °C -20 °C) *4.2 joule/gram °C= 7560J
The unknown substance is added to the water, so its final temperature should be the same as the water. The calculation would be:
7560J= 124g * (100-26)* specific heat
specific heat= 7560J / 124g / 74 °C= 0.8238 J/gram °C 
 
        
             
        
        
        
Answer:
1) 2.054 x 10⁻⁴ mol/L.
2) Decreasing the temperature will increase the solubilty of O₂ gas in water.
Explanation:
1) The solubility of O₂ gas in water:
- We cam calculate the solubility of O₂ in water using Henry's law: <em>Cgas = K P</em>,
- where, Cgas is the solubility if gas,
- K is henry's law constant (K for O₂ at 25 ̊C is 1.3 x 10⁻³ mol/l atm),
- P is the partial pressure of O₂ (P = 120 torr / 760 = 0.158 atm).
- Cgas = K P = (1.3 x 10⁻³ mol/l atm) (0.158 atm) = 2.054 x 10⁻⁴ mol/L.
2) The effect of decreasing temperature on the solubility O₂ gas in water:
- Decreasing the temperature will increase the solubilty of O₂ gas in water.
- When the temperature increases, the solubility of O₂ gas in water will decrease because the increase in T will increase the kinetic energy of gas particles and increase its motion that will break intermolecular bonds and escape from solution.
- Decreasing the temperature will increase the solubility of O₂ gas in water will because the kinetic energy of gas particles will decrease and limit its motion that can not break the intermolecular bonds and increase the solubility of O₂ gas.
 
        
                    
             
        
        
        
<h2>
Answer</h2>
Bromination:
Any reaction or process in which bromine (and no other elements) are introduced into a molecule.
Bromonium Ion:
The bromonium ion is formed when alkenes react with bromine. When the π cloud of the alkene (acting as a nucleophile) approaches the bromine molecule (acting as an electrophile), the σ-bond electrons of Br2 are pushed away, resulting in the departure of the bromide anion.(2)
Mechanism:
Step 1:
In the first step of the reaction, a bromine molecule approaches the electron-rich alkene carbon–carbon double bond. The bromine atom closer to the bond takes on a partial positive charge as its electrons are repelled by the electrons of the double bond. The atom is electrophilic at this time and is attacked by the pi electrons of the alkene [carbon–carbon double bond]. It forms for an instant a single sigma bond to both of the carbon atoms involved (2). The bonding of bromine is special in this intermediate, due to its relatively large size compared to carbon, the bromide ion is capable of interacting with both carbons which once shared the π-bond, making a three-membered ring. The bromide ion acquires a positive formal charge. At this moment the halogen ion is called a "bromonium ion".
Step 2:
When the first bromine atom attacks the carbon–carbon π-bond, it leaves behind one of its electrons with the other bromine that it was bonded to in Br2. That other atom is now a negative bromide anion and is attracted to the slight positive charge on the carbon atoms. It is blocked from nucleophilic attack on one side of the carbon chain by the first bromine atom and can only attack from the other side. As it attacks and forms a bond with one of the carbons, the bond between the first bromine atom and the other carbon atoms breaks, leaving each carbon atom with a halogen substituent.
In this way the two halogens add in an anti addition fashion, and when the alkene is part of a cycle the dibromide adopts the trans configuration.