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RSB [31]
2 years ago
8

The theoretical yield of NaBr from

Chemistry
1 answer:
Dvinal [7]2 years ago
5 0

the percent yield of the reaction is 100%.

The percent yield is calculated as the experimental yield divided by the theoretical yield x 100%:

% yield = actual yield / theoretical yield * 100%

% yield of a reaction in this case Rate

In this case, the molar mass of NaBr is 102.9 g / mol, as you know:

444 actual yield = 7.08 mol x 102.9 g / mol = 728.532 g

theoretical yield = 7.08 mol x 102.9 g / mol = 728.532 g

, Replaced by the definition of percent yield:

percent yield = 728.532 grams / 728.532 grams * 100%

percent yield = 100%

Finally, the percent yield of the reaction is 100%.

<h3 />

FeBr3 is iron bromide. Also known as iron bromide. Iron bromide is an ionic compound in which iron is in a +3 oxidation state.

Learn more about % yield here:brainly.com/question/27979178

#SPJ10

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When methyloxirane is treated with HBr, the bromide ion attacks the less substituted position. However, when phenyloxirane is tr
konstantin123 [22]

Answer:

See explanation and picture below

Explanation:

First, in the case of methyloxirane (Also known as propilene oxide) the mechanism that is taking place there is something similar to a Sn2 mechanism. Although a Sn2 mechanism is a bimolecular substitution taking place in only step, the mechanism followed here is pretty similar after the first step.

In both cases, the H atom of the HBr goes to the oxygen in the molecule. You'll have a OH⁺ in both. However, in the case of methyloxirane the next step is a Sn2 mechanism step, the bromide ion will go to the less substitued carbon, because the methyl group is exerting a steric hindrance. Not a big one but it has a little effect there, that's why the bromide will rather go to the carbon with more hydrogens. and the final product is formed.

In the case of phenyloxirane, once the OH⁺ is formed, the next step is a Sn1 mechanism. In this case, the bond C - OH⁺ is opened on the side of the phenyl to stabilize the OH. This is because that carbon is more stable than the carbon with no phenyl. (A 3° carbon is more stable than a 2° carbon). Therefore, when this bond opens, the bromide will go there in the next step, and the final product is formed. See picture below for mechanism and products.

4 0
3 years ago
A tire at 21°C has a pressure of 0.82 atm. Its temperature decreases to –3.5°C. If there is no volume change in the tire, what i
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a

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Explanation: Hoped this helped! :)

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Answer:

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