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iogann1982 [59]
3 years ago
9

Find the boiling point temperature at 760 torr of an isomer of octane, c8h18, if its enthalpy of vaporization is 38,210 j mol-1

and its vapor pressure at 110.0°c is 638.43 torr.
Chemistry
1 answer:
mixas84 [53]3 years ago
7 0

According to Clausius-Clayperon equation,

ln(\frac{P_{1} }{P_{2} }) = \frac{delta H_{vap} }{R} (\frac{1}{T_{2} }-\frac{1}{T_{1} }   )

P_{1}is the vapor pressure at boiling point = 760 torr

P_{2} is the vapor pressure at T_{2} =638.43 torr

TemperatureT_{2} = 110.0^{0}C + 273 = 383 K

ΔH_{vap} = 38210 J/mol

Plugging in the values, we get

ln(\frac{P_{1} }{P_{2} }) = \frac{delta H_{vap} }{R} (\frac{1}{T_{2} }-\frac{1}{T_{1} }   )

ln\frac{760 torr}{638.43 torr} =\frac{38210 J/mol}{8.314 J/(mol.K)} (\frac{1}{383 K}-\frac{1}{T_{1} }

T_{1} = 389 K

Therefore, the boiling point of octane = 389 K - 273 = 116^{0}C

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Alex_Xolod [135]

The pH = 2.41

<h3>Further explanation</h3>

Given

5.0% by mass solution of acetic acid

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Required

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Solution

Molarity of solution :

\tt M=\dfrac{\%mass\times \rho\times 10}{MW~acetic~acid}\\\\M=\dfrac{5\times 1.007\times 10}{60}\\\\M=0.839

Ka for acetic acid = 1.8 x 10⁻⁵

[H⁺] for weak acid :

\tt [H^+]=\sqrt{Ka.M}

Input the value :

\tt [H^+]=\sqrt{1.8\times 10^{-5}\times 0.839}\\\\(H^+]=0.00388=3.88\times 10^{-3}\\\\pH=3-log~3.88=2.41

7 0
3 years ago
What material was added to powdered rock during tuttle and bowen's experiments?
Rzqust [24]

Answer:

water was added to powdered rock

Explanation:

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xenn [34]

Answer:

a) 2-bromopyrrole

Explanation:

Our options for this questions are:

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b) 2,3-dibromopyrrole

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To understand how the reaction works we have to start with the <u>resonance structures</u>. (Figure 1), on these structures, we will obtain a n<u>egative charge on carbon 2</u> in the pyrrole ring, therefore on this carbon we can generate an attack to an electrophile.

The second step is to check how the mechanism take place. An <u>electrophile is generated</u> by the Br_2 and FeBr_3. This electrophile can be <u>attacked</u> by the negative charge on carbon 2 producing the 2-bromopyrrole. (See figure 2).

I hope it helps!

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Taking advantage of their large differences in pKa values, describe how a mixture of phenol and benzoic acid in diethyl ether so
Marat540 [252]

Answer:

By adding bicarbonate.

Explanation:

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C₆H₅-COOH + HCO₃⁻  ⇄  C₆H₅-COO⁻  +  H₂CO₃

C₆H₅-OH + HCO₃⁻  ⇄  no reaction

The reaction of the benzoic acid with bicarbonate will produce the benzoate ion that will be soluble in the aqueous layer, while the phenol will remain dissolved in the organic layer, so we can separate the two of them by the separation of the two immiscible layers.      

Having the two layers separated, the benzoic acid can be recovered from the aqueous layer by adding HCl:

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<u>This acid will precipitate from the aqueous solution, and the solid can be isolated by filtration</u>.  

The phenol in the organic layer can be dissolved into an aqueous layer by the adding of a strong base like NaOH:

C₆H₅-OH + OH⁻  ⇄  C₆H₅-O⁻ + H₂O

The phenoxide ion soluble in the aqueous layer can be recovered later by the adding of HCl, which will form the original phenol:

C₆H₅-O⁻ + HCl  ⇄  C₆H₅-OH + Cl⁻  

<u>The precipitated phenol can be isolated by filtration. </u>

This way we can separate a mixture of phenol and benzoic acid in diethyl ether solution.  

I hope it helps you!

6 0
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