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8 days ago
13

The average bond energy (enthalpy) for a C=C double bond is 614 kJ/mol and that of a C−C single bond is 348 kJ/mol. Estimate the

energy needed to break only the π bond of the double bond of 2-butene. Express your answer numerically in joules per molecule.
Chemistry
1 answer:
eduard [2.5K]8 days ago
7 0
4.42x10⁻¹⁹ J/molecule Explanation: In a double bond, both sigma and pi bonds exist, while a single bond comprises only a sigma bond. Given that breaking both bonds requires 614 kJ/mol, while breaking just the sigma bond needs 348 kJ/mol, the energy specific to breaking the pi bond is calculated as E = 614 - 348 = 266 kJ/mol. Since 1 kJ equates to 1000 J, this correlates to 266,000 J/mol. With Avogadro's number (1 mol = 6.02x10²³ molecules), we calculate E = 266,000 J/mol * (1 mol/6.02x10²³ molecules) yields E = 4.42x10⁻¹⁹ J/molecule.
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An atom of beryllium (m = 8.00 u) splits into two atoms of helium (m = 4.00 u) with the release of 92.2 kev of energy. if the or
VMariaS [2693]
The energy released results in a kinetic energy of 92.2 keV for the products. We should convert keV into Joules, noting that 1 keV equals a kiloelectron volt. The required conversion is: 1.602×10⁻¹⁹ <span>joule = 1 eV

Kinetic energy = 92.2 keV * (1,000 eV/1 keV) * (</span>1.602×10⁻¹⁹ joule/1 eV) = 5.76×10²³ Joules

Next, we can determine the velocity of each He atom from the kinetic energy:
KE = 1/2*mv²
5.76×10²³ Joules = 1/2*(4)(v²)
This solves to give us: v = 5.367×10¹¹ m/s
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9 days ago
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A sample of solid naphthalene is introduced into an evacuated flask. Use the data below to calculate the equilibrium vapor press
Tems11 [2403]

Answer: The vapor pressure of naphthalene within the flask remains at 2.906\times 10^{-4} atm.

Explanation:

The transformation from solid naphthalene to its gaseous form follows the equilibrium reaction:

C_{10}H_8(s)\rightleftharpoons C_{10}H_8(g)

  • The formula employed to determine the enthalpy change for the reaction is:  

\Delta H^o_{rxn}=\sum [n\times \Delta H^o_f(product)]-\sum [n\times \Delta H^o_f(reactant)]

The formula for calculating the enthalpy change regarding the aforementioned reaction is:

\Delta H^o_{rxn}=(1\times \Delta H^o_f_{(C_{10}H_8(g))})-(1\times \Delta H^o_f_{(C_{10}H_8(s))})

The provided information includes:

\Delta H^o_f_{(C_{10}H_8(s))}=78.5kJ/mol\\\Delta H^o_f_{(C_{10}H_8(g))}=150.6kJ/mol

Substituting the values into the previous equation produces:

\Delta H^o_{rxn}=(1\times 150.6)-(1\times 78.5)=72.1kJ/mol

  • The formula utilized to compute Gibbs free energy change is of a reaction:

\Delta G^o_{rxn}=\sum [n\times \Delta G^o_f(product)]-\sum [n\times \Delta G^o_f(reactant)]

The equation for the enthalpy change for the reaction is:

\Delta G^o_{rxn}=(1\times \Delta G^o_f_{(C_{10}H_8(g))})-(1\times \Delta G^o_f_{(C_{10}H_8(s))})

The given factors include:

\Delta G^o_f_{(C_{10}H_8(s))}=201.6kJ/mol\\\Delta G^o_f_{(C_{10}H_8(g))}=224.1kJ/mol

By inserting values from the above equation, we arrive at:

\Delta G^o_{rxn}=(1\times 224.1)-(1\times 201.6)=22.5kJ/mol

  • For the calculation of K_1 (at 25°C) regarding the provided value of Gibbs free energy, the following relationship is applied:

\Delta G^o=-RT\ln K_1

where,

\Delta G^o = Gibbs free energy = 22.5 kJ/mol = 22500 J/mol  (Conversion factor: 1kJ = 1000J)

R = Gas constant = 8.314J/K mol

T = temperature = 25^oC=[273+25]K=298K

K_1 = equilibrium constant at 25°C =?

Inserting values into the above equation yields:

22500J/mol=-(8.314J/Kmol)\times 298K\times \ln K_1\\\\K_1=1.14\times 10^{-4}

  • To determine the equilibrium constant at 35°C, we refer to the equation proposed by Arrhenius, which states:

\ln(\frac{K_2}{K_1})=\frac{\Delta H}{T}(\frac{1}{T_1}-\frac{1}{T_2})

where,

K_2 = Equilibrium constant at 35°C =?

K_1 = Equilibrium constant at 25°C = 1.14\times 10^{-4}

\Delta H = Enthalpy change of the reaction = 72.1 kJ/mol = 72100 J

R = Gas constant = 8.314J/K mol

T_1 = Initial temperature = 25^oC=[273+25]K=298K

T_2 = Final temperature = 35^oC=[273+35]K=308K

By plugging values into the equation above, we obtain:

\ln(\frac{K_2}{1.14\times 10^{-4}})=\frac{72100J/mol}{8.314J/K.mol}(\frac{1}{298}-\frac{1}{308})\\\\K_2=2.906\times 10^{-4}

  • In order to calculate the partial pressure of naphthalene at 35°C, we utilize the equation for K_p, which is:

K_p=\frac{p_{C_{10}H_8(g)}}{p_{C_{10}H_8(g)}}=p_{C_{10}H_8(g)

The partial pressure of the solid phase is considered to be 1 at equilibrium.

Therefore, the value for K_2 will equal K_p

p_{C_{10}H_8}=2.906\times 10^{-4}

Consequently, the partial pressure of naphthalene at 35°C is 2.906\times 10^{-4} atm.

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8 days ago
At what temperature would the volume of a gas be 0.550 L if it had a volume of 0.432 L at –20.0 o C?
castortr0y [2743]
To find the temperature at which the volume of the gas would be 0.550 L, given that it is 0.432 L at -20.0 °C, apply Charles’s Law.

The formula is v1/T1 = v2/T2
Known values:
V1 = 0.550 L
T1 = ?
T2 = -20°C + 273 = 253 K
V2 = 0.432 L

Rearranging for T1:
T1 = (V1 × T2) / V2

Calculating:
T1 = (0.55 L × 253) / 0.432 L = 322.11 K or 49.11°C
8 0
1 month ago
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The two-slit diffraction experiment shows how light can be treated as particles and how light waves carry the statistical inform
alisha [2718]

The double-slit experiment serves as a renowned method to exemplify concepts in quantum mechanics. Specifically, it highlights the idea of wave-particle duality. Employing a light wave shows diffraction and interference, which are typical characteristics of wave behavior. Unexpectedly, using an electron beam produces an interference pattern as well, indicating that electrons can exhibit wave-like properties.


Explanation:

The optical phenomenon would nearly resemble, yet be entirely distinct from, that involved with the exploitation of light. Interference and diffraction are the characteristics distinguishing waves from particles: waves can interfere and disperse, whereas particles cannot.

Light curves around obstacles akin to waves, and this bending results in the single-slit diffraction pattern.

5 0
21 day ago
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A stock solution of Cu2+(aq) was prepared by placing 0.8875 g of solid Cu(NO3)2∙2.5 H2O in a 100.0-mL volumetric flask and dilut
Anarel [2605]

Answer:

3.816 × 10⁻³ M

Explanation:

A stock solution of Cu²⁺(aq) is made by dissolving 0.8875 g of solid Cu(NO₃)₂∙2.5H₂O in a 100.0-mL volumetric flask, and then brought up to volume with water. What is the molarity (in M) of Cu²⁺(aq) in this stock solution?

We can derive the following relations:

  • The molar mass of Cu(NO₃)₂∙2.5H₂O is 232.59 g/mol.
  • Each mole of Cu(NO₃)₂∙2.5H₂O yields one mole of Cu²⁺.

The moles of Cu²⁺ present in 0.8875 g of Cu(NO₃)₂∙2.5H₂O are:

0.8875gCu(NO_{3})_{2}.2.5H_{2}O\times \frac{1molCu(NO_{3})_{2}.2.5H_{2}O}{232.59gCu(NO_{3})_{2}.2.5H_{2}O} \times \frac{1molCu^{2+} }{1molCu(NO_{3})_{2}.2.5H_{2}O} =3.816\times10^{-3} molCu^{2+}

The molarity of Cu²⁺ is:

\frac{3.816\times10^{-3} mol}{100.0 \times10^{-3}L} =3.816\times10^{-2}M

4 0
20 days ago
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