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Lynna [10]
3 years ago
11

Explain how you would make up a one molar (1m) solution of ethyl alcohol.

Chemistry
1 answer:
Nookie1986 [14]3 years ago
6 0

The formula of molarity is:

molarity = \frac{number of moles of solute}{volume of solution in Liter}

Number of moles is given as:

number of moles of solute= \frac{mass of solute}{Molar mass of solute}

So, the formula of molarity can be written as:

molarity = \frac{\frac{mass of solute}{Molar mass of solute}}{volume of solution in Liter}    -(1)

Molar mass of ethyl alcohol, C_2H_5OH = 2\times 12+6\times 1+16 = 46 g/mol

Molarity of ethyl alcohol, C_2H_5OH = 1 molar  (given)

Let the volume of solvent that is water be 1 L.

Substituting the values in formula (1):

1 M = \frac{\frac{mass of solute}{46 g/mol}}{1 L}

mass of solute = 46 g/mol\times 1 mol/L\times 1 L

mass of solute = 46 g

Since, ethyl alcohol is liquid in room temperature:

Density of ethyl alcohol is 0.7892 g/mL

Density = \frac{mass}{volume}

So, volume of ethyl alcohol = \frac{mass of ethyl alcohol}{density of ethyl alcohol}

Volume of ethyl alcohol = \frac{46 g}{0.7892 g/mL}

Volume of ethyl alcohol = 58.29 mL

Hence, by dissolving 58.29 mL of ethyl alcohol in 1 L of water, 1 M solution of ethyl alcohol can be prepared.

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Explanation:

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How many moles are in 13.0 grams of water​
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4 years ago
What carboxylic acid would be formed if the malonic ester synthesis (alkylation of diethyl malonate followed by hydrolysis with
uranmaximum [27]

Answer:

cyclohexilic acid

Explanation:

The malonic ester synthesis is often used to form different types of carboxilic acid. In this case, we have excess of base, so we can expect a ring formed in the molecule.

In the first step, the base substract the more acidic hydrogen of the ester. In the next step we have the ester reacting with the dibromopentane. Then, in the next step, the excess of base will substract again the acidic hydrogen remaining of the carbon, and then, will promove a Sn2 reaction with the bromine in the pentane (That it was previously attached to the molecule). In this step, a ring id formed. Then, the hydrolisis with acid, will form carboxilic acid in both sides of the molecule, and finally the decarboxilation in heat will separate the molecule and formed the cyclohexilic acid.

The picture below shows the mechanism

3 0
4 years ago
1) Compounds Y and Z both have the formula C9H18.
sashaice [31]

Answer:

See explanation and images attached

Explanation:

We know that the cis isomer has more heat of hydrogenation since it is less stable than the trans isomer. Since the hydrogenation of both compounds yields the same product and the hydroboration/oxidation both give a primary alcohol, they are geometric isomers and Y is the trans isomer (Image 2).

For the compound C8H12, the compound in question must be 1,5- cyclooctadiene since two moles of the same aldehyde was obtained after ozonolysis and reaction with two equivalents of hydrogen gives cyclooctane (Image 1).

5 0
3 years ago
Classify each of the following possible reactions according to whether a precipitate will form or will not form.
elena-14-01-66 [18.8K]

Answer:

Reactions, 2, 3 and 5 make precipitates

Explanation:

1. The halogens always make aqueous salts with elements from group 1

2. Phosphate anion can make insoluble salts, the same as carbonate.

3. Nitrate anion always make aqueous salts

4. Sulfate anion makes aqueous salts except with Ag⁺, Pb⁺² and group 2

1. KI(aq) + NaCl(aq) → KCl(aq) + NaI(aq)

2. 2Na₃PO₄ (aq) + 3CoCl₂(aq) → 6NaCl(aq) + Co₃(PO₄)₂(s) ↓

3. Na₂CO₃ (aq) + CuCl₂ (aq) → 2NaCl (aq) + CuCO₃ (s) ↓

4. 2LiNO₃ (aq) + Na₂SO₄ (aq) → Li₂SO₄ (aq) + 2NaNO₃(aq)

5.  CrCl₂ (aq) + Li₂CO₃ (aq) → 2LiCl (aq) + Cr₂(CO₃)₂ (s) ↓

8 0
3 years ago
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