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Snowcat [4.5K]
3 years ago
13

Will give brainliest, Look at the graph above. Compare it to the periodic table. What do you notice about the location on the pe

riodic table of the elements that represent the high points

Chemistry
1 answer:
Tatiana [17]3 years ago
3 0

Answer:

We can see that the atomic radius decreases across every row.

Explanation:

I will comment more below.

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Which of the following are units for energy? Gram, joule, kilogram, calorie
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Calculate the unknown quantity in each of the following measurements of gases ?
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5 0
4 years ago
Use the reaction equation and bond energies to answer the question.
Arisa [49]

This problem is providing us with the chemical equation for the decomposition of water to hydrogen and oxygen, the involved bond energies and asks for the total energy of the reaction as well as whether it is endothermic or exothermic. At the end, one comes to the conclusion that  it is exothermic because the total energy is -425 kJ.

<h3>Bond energy:</h3>

In chemistry, bond energies are defined as the necessary energy to break a bond between two atoms. In this case, we see that water, H2O has two H-O bonds and hydrogen and oxygen have two H-H and one O=O bonds, respectively.

Thus, we write the following heat equation, which comprises the aforementioned bond energies and the stoichiometric coefficients in the reaction:

\Delta H=2*\Delta H_{H-O}-(2*\Delta H_{H-H}+\Delta H_{O=O})

Hence, we plug in the given bond energies to obtain:

\Delta H=2*467kJ/mol-(2*432kJ/mol+495kJ/mol)\\&#10;\\&#10;\Delta H =-425kJ/mol

Where the negative suggests this is an exothermic reaction as it releases energy (negative enthalpy).

Learn more about bond energies: brainly.com/question/26141360

5 0
3 years ago
A molecule and its chair flip are related by being labled as
Nezavi [6.7K]

A molecule and its chair flip are related by being labled as Conformational isomers

The process of rotating around single bonds to change one cyclohexane chair conformation into another. Axial substituents become equatorial upon cyclohexane ring flip, whereas equatorial substituents become axial.

<h3>What is Conformational isomers ?</h3>

Stereoisomers created by rotation (twisting) about -bonds are known as conformational isomers (also known as conformers, rotational isomers, or rotamers), and they frequently interconvert quickly at room temperature.

  • For instance, butane contains three conformers related to its two methyl (CH3) groups: two gauche conformers with enantiomeric methyls that are spaced 60 degrees apart, and an anti conformer with coplanar four carbon centres and 180-degree-spaced substituents (refer to free energy diagram of butane).

Learn more about Conformational isomers here:

brainly.com/question/15107036

#SPJ9

8 0
2 years ago
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