Answer:

Explanation:
The volume and amount of gas are constant, so we can use Gay-Lussac’s Law:
At constant volume, the pressure exerted by a gas is directly proportional to its temperature.

Data:
p₁ =5.7 atm; T₁ = 100.0 °C
p₂ = ?; T₂ = 20.0 °C
Calculations:
1. Convert the temperatures to kelvins
T₁ = (100.0 + 273.15) K = 373.15
T₂ = (20.0 + 273.15) K = 293.15
2. Calculate the new pressure

Answer:
pH = 2.69
Explanation:
The complete question is:<em> An analytical chemist is titrating 182.2 mL of a 1.200 M solution of nitrous acid (HNO2) with a solution of 0.8400 M KOH. The pKa of nitrous acid is 3.35. Calculate the pH of the acid solution after the chemist has added 46.44 mL of the KOH solution to it.</em>
<em />
The reaction of HNO₂ with KOH is:
HNO₂ + KOH → NO₂⁻ + H₂O + K⁺
Moles of HNO₂ and KOH that react are:
HNO₂ = 0.1822L × (1.200mol / L) = <em>0.21864 moles HNO₂</em>
KOH = 0.04644L × (0.8400mol / L) = <em>0.0390 moles KOH</em>
That means after the reaction, moles of HNO₂ and NO₂⁻ after the reaction are:
NO₂⁻ = 0.03900 moles KOH = moles NO₂⁻
HNO₂ = 0.21864 moles HNO₂ - 0.03900 moles = 0.17964 moles HNO₂
It is possible to find the pH of this buffer (<em>Mixture of a weak acid, HNO₂ with the conjugate base, NO₂⁻), </em>using H-H equation for this system:
pH = pKa + log₁₀ [NO₂⁻] / [HNO₂]
pH = 3.35 + log₁₀ [0.03900mol] / [0.17964mol]
<h3>pH = 2.69</h3>
Answer:
True
Explanation:
the machine shown in figure 9.9 is called a wheele and axle. It's a form of lever. the effort arm can rotate in a complete circle, which is the center of the axle.
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.