Which of the following solutions has the highest concentration of sugar?

A mover packs books, CDs, and DVDs into a moving box. If the box contains 6.5 kg of books, 1.5 kg of CDs, and 2.0 kg of DVDs, wh

mariarad [96]

Given:
M1 = 6.5 kg of books
M2 = 1.5 kg of CDs
M3 = 2.0 kg of DVDs

Required: percent by mass of each object

Solution:
First, we calculate the total mass.

M = 6.5 kg + 1.5 kg + 2.0 kg = 10 kg

Percent by mass is calculated by getting the ration of the mass of an object and the total mass multiplied by 100 to get the percent.

%M1 = 6.5 / 10 x 100 = 65%
%M2 = 1.5/10 x 100 = 15%
%M3 = 2.0/10 x 100 = 20%

4 0

3 years ago

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When bridges are built, special joints must be used because the material of the bridge shrinks, and without these joints, the ma

marysya [2.9K]

Expansion

Explanation:

Expansion is the change is size of a body with increasing temperature and tension.

Bridges are built of iron. Iron thermally expands in the presence of increased temperature during the day. The length of the iron will increase by simple fractions. At night, when temperature drops, the bar returns back to its initial position.

The allowance for expansion of the metal is made in order to prevent tension within the structure.
Not doing this will cause the material to break since there is no free space for the bar to change shape.

Learn more:

Expansion in gases brainly.com/question/9979757

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6 0

3 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.