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Lady bird [3.3K]
1 year ago
8

How are large polymers formed? by repetitive combinations of simple subunits by the addition of halogens to a small molecule by

combining a few different and larger molecules by combining many different and smaller molecules
Chemistry
1 answer:
Gre4nikov [31]1 year ago
6 0

Answer:

How are large polymers formed? by repetitive combinations of simple subunits by the addition of halogens to a small molecule by combining a few different and larger molecules by combining many different and smaller molecules

Explanation:

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The equilibrium concentrations of the reactants and products are [ HA ] = 0.260 M [HA]=0.260 M , [ H + ] = 2.00 × 10 − 4 M [H+]=
ValentinkaMS [17]

Answer:

pKa of the acid HA with given equilibrium concentrations is 6.8

Explanation:

The dissolution reaction is:

HA ⇔ H⁺ + A⁻

So at equilibrium, Ka is calculated as below

Ka = [H⁺] x [A⁻] / [HA] = 2.00 x 10⁻⁴ x 2.00 x 10⁻⁴ / 0.260

    = 15.38 x 10⁻⁸

Hence, by definition,

pKa = -log(Ka) = - log(15.38 x 10⁻⁸) = 6.813

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Complete the following chart to fill in the blanks
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Which event must always occur for a chemical reaction to occur
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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.

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