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dsp73
2 years ago
8

A given sample of caffeine, C8H10N4O2, has 6.47 x 1022

Chemistry
1 answer:
Verdich [7]2 years ago
3 0

Answer:

<u>8.08 × </u>10^{22}<u> atoms of hydrogen</u>

Explanation:

From the given data, we have two categories of variables (unknowns):

  • Amount (moles or mass) of Caffeine
  • Amount (moles or mass) of Hydrogen

The longer route would be to solve for these variables first, by determining the number of moles of the Caffeine sample (0.134 moles of C8H10N4O2) from the mass of carbon (12.89 g = 1.07 moles in 6.47 10^{22} atoms) provided. And then solve for the number of atoms of H. <u><em>[N.B: 1 mole of ANY substance = 6.022 × </em></u>10^{22}<u><em> atoms ]</em></u>

Alternatively and quicker, we can use the mole ratios of the Carbon:Hydrogen atoms in the compound.

8 : 10 ≡ 4 : 5

If   4 moles -- 6.47 10^{22} atoms

Then 5 moles -- ?? atoms

⇒ No. of atoms of Hydrogen = \frac{5*6.47*10^{22}}{4}

<u>=8.08 × </u>10^{22}<u> atoms of hydrogen</u>

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2 years ago
Identify the most and the least acidic compound in each of the following sets.
il63 [147K]

Answer:

See explanation

Explanation:

Our answer options for this question are:

a. 2-chlorobutanoic acid:_______ 2-chlorobutanoic acid:_______ 3-chlorobutanoic acid:______.

b. 2,4-dinitrobenzoic acid:______ p-nitrobenzoic acid:______ p-bromobenzoic acid:_______.

c. p-cyanobenzoic acid:________ benzoic acid:_______ p-aminobenzoic acid:______

We have to check each set of molecules

<u>a. 2-chlorobutanoic acid,</u> <u>3-chlorobutanoic acid</u>

<u />

In this case, the difference between these molecules is the position of "Cl". If the chlorine atom is closer to the acid group, we will have a higher inductive effect. So, the bond O-H would be weaker and we will have more acidity. So, the molecule with more acidity is <u>2-chlorobutanoic acid</u> and the less acidic would be <u>3-chlorobutanoic acid.</u>

<u />

<u>b. 2,4-dinitrobenzoic acid,</u> <u>p-nitrobenzoic acid,</u> <u>p-bromobenzoic acid</u>

<u />

In this case, we have several structural differences. In all the structure, we have deactivating groups (Br and NO_2). If we have a deactivating group the acidity will increase. In the case of "Br", we have a weak deactivating, so, this will be the less acidic one (<u>p-bromobenzoic acid)</u>

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<u>c. p-cyanobenzoic acid</u>, <u>benzoic acid</u>, <u>p-aminobenzoic acid</u>

On these molecules, we have several structural differences. In <u>p-cyanobenzoic acid</u> we have a deactivating group, therefore in this molecule we will have more acidity. In the <u>p-aminobenzoic acid,</u> we have an activating group, so, this would be the less acidic compound.

<u />

See figure 1

I hope it helps!

<u />

<u />

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Tpy6a [65]

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