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Assoli18 [71]
3 years ago
14

Consider the reaction:

Chemistry
1 answer:
ruslelena [56]3 years ago
8 0

Answer:

Co2 answer

Explanation:

just add them all you will be able to get the answer

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HELPP ME ASAP<br> What is the percent composition of Nitrogen in dinitrogen trioxide?
Arte-miy333 [17]
28% is the answer i got
7 0
3 years ago
5. Which statement is true about electronegativity?
Anit [1.1K]

Answer:

Electronegativity generally increases from left to right across a period,

Explanation:

The true statement from the given choices is that electronegativity generally increases from left to right across a period.

Electronegativity is the measure of the relative tendency with which an atom of the element attract valence electrons in a chemical bond.

Across a period electronegativity increases from left to right and decreases down the group.

This is due to reduction in metallic properties as we move across the period from left to right.

3 0
3 years ago
You could also graph decay time (in seconds or minutes) vs. number of radioactive nuclei. How would this graph differ from the g
Tatiana [17]
Only one of the listed choices are correct here:
<span><em>The x-axis would change title and values.</em>
</span>
6 0
3 years ago
Read 2 more answers
1. Stirring increases the rate of solution
Blababa [14]

Answer:

1) <em>The correct answer is A. Collision</em>

2) A hot solvent helps a solid dissolve faster because an increase in <u><em>kinetic energy</em></u> that also increases the rate of collisions

Explanation:

When a solute is added into a solvent and stirred, the solute particles get distributed to all parts of the solvent as a result of stirring.

More collisions occur between the solute and the solvent due to stirring. This increases the rate of dissolving.

<em>When a solvent is heated, then the kinetic energy would increase and the atoms will collide with a much greater force. As a result, ore solute will be able to dissolve in the solvent. </em>

3 0
3 years ago
Functional group and bond hybridization of vanillin
lana66690 [7]

Vanillin is the common name for 4-hydroxy-3-methoxy-benzaldehyde.

See attached figure for the structure.

Vanillin have 3 functional groups:

1) aldehyde group:  R-HC=O, in which the carbon is double bonded to oxygen

2) phenolic hydroxide group: R-OH, were the hydroxyl group is bounded to a carbon from the benzene ring

3) ether group: R-O-R, were hydrogen is bounded through sigma bonds to carbons

Now for the hybridization we have:

The carbon atoms involved in the benzene ring and the red carbon atom (from the aldehyde group) have a <u>sp²</u> hybridization because they are involved in double bonds.

The carbon atom from the methoxy group (R-O-CH₃) and the blue oxygen's have a  <u>sp³</u>  hybridization because they are involved only in single bonds.

7 0
3 years ago
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