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Alexeev081 [22]
3 years ago
13

Which of these is a chemical property?

Chemistry
2 answers:
ankoles [38]3 years ago
7 0

Answer:

The second choice, or flammability.

Explanation:

The flammability of something is how easy it is for it to burn or ignite.

Marat540 [252]3 years ago
6 0

Answer:

The Answer in flammability

Explanation:

Both fire and the fire starter are chemicals therefore its B.

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Which elements did you include in your question?
SIZIF [17.4K]

Answer:

It should be all of them

Explanation:

It’s because it was in your question you wrote out

3 0
2 years ago
What happens to the light ray when it hits the boundary between water and glass
torisob [31]

Answer: If the light ray hits the boundary at an angle which is not perpendicular to or parallel to the surface, then it will change direction and appear to `bend'

Hope This Helps You! :D

6 0
3 years ago
Why don't noble gases bond?
Luba_88 [7]
<span>Their outer shells are filled So much that they don't need to bond or react with any other atoms.</span>
7 0
3 years ago
HELP ME!!ILL GIVE U BRAINLIESTT!!!!!
Elodia [21]
It’s the nerves but I’m not 100% sure if I’m correct
6 0
3 years ago
Predict the two most likely mechanisms for the reaction of 1-iodohexane with potassium tert-butoxide.
Rudiy27

Answer:

C) SN2 and E2

Explanation:

For this question, we have analyzed the <u>substrate</u> and the <u>base/nucleophile</u>. The substrate, in this case, is 1-iodohexane and the base/nucleophile is potassium tert-butoxide.

<u>Substrate</u>

<u />

In the 1-iodohexane the iodide "I" is bonded to a primary carbon (carbon 1). Therefore we will have a <u>primary substrate</u>. If we have a primary substrate an Sn1 can not take place. We can not have a <u>primary carbocation</u> due to this instability. So, we can disccard options A) and B).

<u>Base/nucleophile</u>

<u />

In the potassium tert-butoxide we have an ionic compound. A positive charge is placed in the potassium atom a negative charge is placed in the oxygen of the ter-butoxide ion. So, we will have a <u>strong base</u> (a molecule with the ability to remove electrons) and a <u>strong nucleophile</u> (a molecule with ability to bond with an electrophile). With all this in mind, w<u>e can not have an E1 reaction</u>.

With both analyses, the answer is C).

See figure 1

I hope it helps!

6 0
3 years ago
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