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2 years ago

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A 2.0 L sample of nitrogen gas is at a pressure of 1.0 atm. What will be the pressure of the gas if the volume is reduced to 0.2

5 L?

1 answer:

Bad White [126]2 years ago

4 0

Answer:

8 ATM

Explanation:

P1 V1 = P2 V2

P1 V1 / V2 = P2

1 * 2 / .25 = 8 ATM

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isotopes of an element have the same number of protons but a different number of neutrons below u will see the nucleus of four d

dexar [7]

What is your question? Its not clear

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3 years ago

Use bond energies from Table 10.3 in the textbook to estimate the enthalpy change (ΔH) for the following reaction. C2H2(g)+H2(g)

Digiron [165]

Answer: $=176.6kJmol^{-1}$

Explanation:Bond energy of H-H is 436.4 kJ/mole

Bond energy of C-H is 414 kJ/mol

Bond energy of C=C is 620 kJ/mol

Bond energy of C≡C is 835 kJ/mol

$\Delta H= {\text {sum of bond energies of reactants}}- {\text {sum of bond energies of products}}$

$\Delta H$ = {1B.E(C≡C)+2B.E(C-H) +1B.E(H-H)} - {1B.E(C=C)+4B.E(C-H)}

$\Delta H= {1B.E(835kJmole^{-1})+2B.E(414kJmole^{-1}) +1B.E(436.4kJmole^{-1})} - {1B.E(620kJmole^{-1})+4B.E(414kjmole^{-1})}$

$=176.6kJmol^{-1}$

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3 years ago

Isotonic compound have high melting point. Why ? Name the ions present in CaS.

yuradex [85]

Explanation:

Because a large amount of energy is required to break the strong inter-ionic attraction.

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3 years ago

Consider the reaction below. HI + H2O mc014-1.jpg H3O+ + I– Which is an acid-conjugate base pair? HI and H2O H2O and H3O+ H3O+ a

lesya692 [45]

Answer: Option (d) is the correct answer.

Explanation:

According to Bronsted-Lowry, species which donate a proton are known as acid. The species which accept a proton are known as a base.

In the given reaction, acids and bases are as follows.

HI + $H_{2}O$ $\rightarrow$ $H_{3}O^{+}$ + $I^{-}$

Acid Base Conjugate acid Conjugate base

Therefore, the acid HI loses a proton to form a conjugate base that is $I^{-}$ .

Thus, we can conclude that HI and $I^{-}$ is an acid conjugate base pair.

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3 years ago

Read 2 more answers

The tosylate of (2R,3S)-3-phenylbutan-2-ol undergoes an E2 elimination on treatment with sodium ethoxide. Draw the structure of

andrezito [222]

Answer:

(R)-but-3-en-2-ylbenzene

Explanation:

In this reaction, we have a very <u>strong base</u> (<em>sodium ethoxide</em>). This base, will remove a hydrogen producing a double bond. We know that the reaction occurs through an <u>E2 mechanism</u>, therefore, the hydrogen that is removed must have an <u>angle of 180º</u> with respect to the leaving group (the "OH"). This is known as the <u>anti-periplanar configuration</u>.

The hydrogen that has this configuration is the one that placed with the <u>dashed bond</u> (<em>red hydrogen</em>). In such a way, that the base will remove this hydrogen, the "OH" will leave the molecule and a double bond will be formed between the methyl and the carbon that was previously attached to the "OH", producing the molecule (R) -but-3- en-2-ylbenzene.

See figure 1

I hope it helps!

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3 years ago