Answer:
-125 kJ
Explanation:
You calculate the energy required to break all the bonds in the reactants. Then you subtract the energy to break all the bonds in the products.
H₂C=CH₂ + H₂ ⟶ H₃C-CH₃
Bonds: 4C-H + 1C=C 1H-H 6C-H + 1C-C
D/kJ·mol⁻¹: 413 612 436 413 347
The formula relating ΔHrxn and bond dissociation energies (D) is
ΔHrxn = Σ(Dreactants) – Σ(Dproducts)
(Note: This is an exception to the rule. All other thermochemical reactions are “products – reactants”. With bond energies, it’s “reactants – products”. The reason comes from the way we define bond energies.)
<em>For the reactant</em>s:
Σ(Dreactants) = 4 × 413 + 1 × 612 + 1 × 436 = 2700 kJ
<em>For the products:</em>
Σ(Dproducts) = 6 × 413 + 1 × 347 = 2825 kJ
<em>For the system</em>
:
ΔHrxn = 2700 - 2825 = -125 kJ
Answer:
a, g, c
Explanation:
The conversion of the stable cyclopentane into Trans-1, 2dibromocyclopentane will require three step reactions.
The first is to convert the compound into a cyclopentene, through the addition of Bromine water under heat and photons (light). So option A is the first in the order. This will generate 1 bromocyclopentane through halogenation of the alkane. Secondly, a hot and strong base should be added like the NaOEt, EtOH to remove the added bromine and one atom of hydrogen from the resulting 1 bromocyclopentane in the previous reaction. This will yield cyclopentene, thus making the compound more electrophilic. So option g is required. Thirdly, bromine molecules will be added (C) to take up their places at the two electrophilic regions of the compound to produce Trans-1, 2dibromocyclopentane.