Answer:
Hydrogen: -141 kJ/g
Methane: -55kJ/g
The energy released per gram of hydrogen in its combustion is higher than the energy released per gram of methane in its combustion.
Explanation:
According to the law of conservation of the energy, the sum of the heat released by the combustion and the heat absorbed by the bomb calorimeter is zero.
Qc + Qb = 0
Qc = -Qb [1]
We can calculate the heat absorbed by the bomb calorimeter using the following expression.
Q = C . ΔT
where,
C is the heat capacity
ΔT is the change in the temperature
<h3>Hydrogen</h3>
Qc = -Qb = -C . ΔT = -(11.3 kJ/°C) . (14.3°C) = -162 kJ
The heat released per gram of hydrogen is:
<h3>Methane</h3>
Qc = -Qb = -C . ΔT = -(11.3 kJ/°C) . (7.3°C) = -82 kJ
The heat released per gram of methane is:
Answer:
V = 85.2
Explanation:
STP = 273K and 1 atm
Considering what we know about STP, we get the moles, temperature, and pressure. Using the ideal gas law we can find the volume (PV = nRT). Plug in our variables: (1 * V = 3.80 * R * 273). Since we are dealing with atm and not kPA or mmHg, we use the constant for atm (0.0821) which we use for R. (So.. now our equation is 1 * V = 3.80 * 0.0821 * 273). We now multiply the right side to get 85.17054. So... V = 85.2 considering sigificant figures (this is the part where I am the least sure of, since I havent done sig figs in a while)
Answer:(4) ----accepts a proton
Explanation:
H2O water can produce both hydrogen and hydroxide ions
H2O --> H+ + OH-
According to the Bronsted-Lowry theory, it can be a proton donor and a proton acceptor.this means that It can donate a hydrogen ion to become its conjugate base, or can accept a hydrogen ion to form its conjugate acid,
When , a water molecule, H2O accepts a proton it will act as a Brønsted-Lowry base especially when dissolved in a strong acidic medium. for eg
HCl + H2O(l) → H3O+(aq) + Cl−(aq)
Here, Hydrochloric acid is a strong acid and ionizes completely in water, since it is more acidic than water, the water will act as a base.
Answer:
1.7 × 10 ^42
Explanation:
Using Nernst equation
E°cell = RT/nF Inq
at equilibrium
Q=K
E°cell = 0.0257 /n Ink= 0.0592/n log K
Fe2+(aq)+2e−→Fe(s) E∘= −0.45 V
Ag+aq)+e−→Ag(s) E∘= 0.80 V
Fe(s)+2Ag+(aq)→Fe2+(aq)+2Ag(s)
balance the reaction
Fe → Fe²⁺ + 2e⁻ reversing for oxidation E° = 0.45 v
2 Ag⁺ +2e⁻ → 2Ag
n = 2 moles and K = equilibrium constant
E° cell = 0.80 + 0.45 = 1.25 V
E° cell = (0.0592 / n) log K
substitute the value into the equations and solve for K
(1.25 × 2) / 0.0592 = log K
42.23 = log K
k = 10^ 42.23
K = 1.7 × 10 ^42
