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GenaCL600 [577]
3 years ago
10

Which of the following is a consequence of humans using fossil fuels

Chemistry
1 answer:
marusya05 [52]3 years ago
8 0

Answer:

Explanation:

Following are a few consequences of fossil fuels

1. It causes air pollution.

2. When they are burned, they produce toxic substances which leads to global warming.

3. Waste products are hazardous to public health and environment.

4. They are non - renewable and unsustainable.

5. Drilling fossil fuels is a dangerous process

Hope this helps

plz mark as brainliest!!!!

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Consider the following reaction: C6H6 + O2 \longrightarrow ⟶ CO2 + H2O 39.7 grams of C6H6 are allowed to react with 105.7 g of O
Ivenika [448]

Answer:

116.3 grCO2

Explanation:

1st - we balance the equation so that it finds the same amount of elements of the product side and of the reagent side

C6H6 +15/2 O2⟶ 6CO2 +3 H2O

2nd - we calculate the limiting reagent

39.2gr C6H6*(240grO2/78grC6H6)=120 grO2

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2 years ago
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.

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3 years ago
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The slope is 10

And the y-intercept is 1

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