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FromTheMoon [43]
3 years ago
13

HELPPPPPPP!!!!!!!!!!

Chemistry
2 answers:
krek1111 [17]3 years ago
8 0
It’s D hope it helps
lorasvet [3.4K]3 years ago
7 0

Answer:

It is D

Explanation:

Im 90% percent sure

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What can be said of a closed system when an exothermic reaction proceeds in an aqueous solution?
lyudmila [28]
An exothermic reaction is a type of reaction that dissipates heat as the reaction proceeds. This would mean that in a closed system, when a reaction proceeds and is endothermic, the temperature of the solution  or the system would increase so as to maintain the equilibrium with the whole system.
8 0
3 years ago
Consider a general reaction
choli [55]

Answer:

a) K = 5.3175

b) ΔG = 3.2694

Explanation:

a) ΔG° = - RT Ln K

∴ T = 25°C ≅ 298 K

∴ R = 8.314 E-3 KJ/K.mol

∴ ΔG° = - 4.140 KJ/mol

⇒ Ln K = - ( ΔG° ) / RT

⇒ Ln K = - ( -4.140 KJ/mol ) / (( 8.314 E-3 KJ/K.mol )( 298 K ))

⇒ Ln K = 1.671

⇒ K = 5.3175

b) A → B

∴ T = 37°C = 310 K

∴ [A] = 1.6 M

∴ [B] = 0.45 M

∴ K = [B] / [A]

⇒ K = (0.45 M)/(1.6 M)

⇒ K = 0.28125

⇒ Ln K = - 1.2685

∴ ΔG = - RT Ln K

⇒ ΔG = - ( 8.314 E-3 KJ/K.mol )( 310 K )( - 1.2685 )

⇒ ΔG = 3.2694

7 0
3 years ago
Products: 1-methylcyclohexene, 3-methylcyclohexene, methylenecyclohexane
Lostsunrise [7]

Answer:

See explanation

Explanation:

The reaction that we are considering here is quite a knotty reaction. It is difficult to decide if the mechanism is actually E1 or E2 since both are equally probable based on the mass of scientific evidence regarding this reaction. However, we can easily assume that the methylenecyclohexane was formed by an E1 mechanism.

Looking at the products, one could convincingly assert that the reaction leading to the formation of the two main products proceeds via an E1 mechanism with the formation of a carbocation intermediate as has been shown in mechanism attached to this answer. Possible rearrangement of the carbocation yields the 3-methylcyclohexene product.

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Gases
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