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Bezzdna [24]
3 years ago
7

How does wax dissolve in kerosene​

Chemistry
1 answer:
Alona [7]3 years ago
6 0

Answer:

Petroleum fractions of this kind are commonly known as kerosene. We find that such a mixture of acetone and kerosene will dissolve parafiin wax more eifectively and rapidly than any other solvent hitherto known, and that the wax, when  dissolved it will remain in liquid condition indefinitely.

Explanation:

i think this is the answer .

please mark as brainliest

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Vinegar is a solution of acetic acid, CH3COOH, dissolved in water. A 5.54-g sample of vinegar was neutralized by 30.10 mL of 0.1
tekilochka [14]

Answer:

3.26 % of vinegar is acetic acid

Explanation:

Step 1: Data given

Mass of the sample = 5.54 grams

Volume of NaOH = 30.10 mL

Molarity of NaOH = 0.100M

Step 2: The balanced equation

CH3COOH + NaOH → CH3COONa + H2O

Step 3: Calculate moles NaOH

Moles NaOH = volume * molarity

Moles NaOH = 0.03010 L * 0.100M

Moles NaOH = 0.00301 moles NaOH

Step 4: Calculate moles CH3COOH

For 1 mol NaOH we need 1 mol CH3COOH

For 0.00301 moles NaOH we nee 0.00301 moles CH3COOH

Step 5: Calculate mass CH3COOH

Mass CH3COOH = moles CH3COOH * molar mass CH3COOH

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7 0
2 years ago
1. Draw a wedge/dash structure for trans-1,2-dimethylcyclohexane.
Angelina_Jolie [31]

Answer:

The structure with the ring flipped is the most stable

Explanation:

We have the  trans 1,2 - dimethylcyclohexane. With the wedge/dash structure we could not figure is this form is stable (If we do a comparison with the cis structure). But when we do a chair structure and ring flipped structure, this is easier to look.

The picture attached shows the structures, they are labeled as 1, 2 and 3, according to this problem.

In the chair structure, according to the picture below, you can see that both methyls are heading in the axial positions of the ring (One facing upward and the other downward). This is pretty stable, however, when the methyls are in those positions, the methyl position 1, can undergoes an 1,3 diaxial interactions with the hydrogens atoms (They are not drawn, but still are there), so this interaction makes this structure a little less stable that it can be.

On the other side, the ring flipped structure, we can see that both methyls are in the equatorials positions of the ring, and in these positions, it can avoid the 1,4 diaxial interactions with the hydrogens atoms, making this structure the most stable structure.

Hope this helps

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