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STALIN [3.7K]
4 years ago
9

In the following reaction, eight moles of sodium hydroxide is broken down into four moles of sodium oxide and four moles of wate

r.
What is the percent error if your experiment yields 195 grams of sodium oxide?
2NaOH→Na2O+H2O
Chemistry
1 answer:
maxonik [38]4 years ago
8 0

Answer:

21.344%

Explanation:

For the given chemical reaction, 8 moles of the reactant should produce 4 moles of Na_{2}O. However, 195 g of Na_{2}O was produced instead. The molar mass of Na_{2}O is 61.9789 g/mol.

Thus, the moles of Na_{2}O produced = 195/61.9789 = 3.1462 moles

The percent error = [(Actual -Experiment)/Actual]*100%

The percent error =  [(4.00 - 3.1462)/4.00]*100% = (0.85376/4.00)*100% = 21.344%

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Answer:

<u>36 times</u>

Explantaion:

The force exerted between two charged particles is directly proportional to the product of the charges and inversely proportional to the square of the distance between them.

In the case of S and q: The distance of separation is 1 unit

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In the case of S and p: the distance is 6 units

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3 years ago
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Answer:

your answer is 30f

Explanation:

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Compound W, C8H17Br, and X, C8H17Cl, are products of the radical bromination (W), and chlorination (X), of 2,4-dimethylhexane. W
oksian1 [2.3K]

Answer:

The possible structures are shown in figure.

Explanation:

The seven isomers that could be formed from the given compound due to radical halogenation are shown in the figure.

We have mentioned only chlorine as group for showing just the chiral nature of the compound.

A chiral compound has a carbon with all the four groups different from each other.

There are three structures which are chiral (as shown).

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X is the chlorinated product.

1) W reacts readily in water to form a chiral substitution product Y, C8H17OH.

Reaction of a single enantiomer of W produces a single enantiomer of Y as the only substitution product.: It means that the substitution is SN2 which is possible if the compund is not tertiary.

2) X likewise reacts readily in water though at a slower rate than W; a chiral substitution product Z, C8H17OH, is again formed. Unlike W, however, reaction of a single enantiomer of X produces Z that is nearly racemic.

It means that it will undergo SN1 reaction,. So the alkyl halide must be tertiary.

The possible structures are shown in figure.

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