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Sidana [21]
2 years ago
8

Does the absolute reference system consider a fixed reference system of reference?

Chemistry
1 answer:
Rufina [12.5K]2 years ago
6 0

Answer:

The definition of an absolute reference frame would be that fixed reference frame that every observer would rest at all times in his/her state of motion.

Explanation:

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2) Will all atoms behave exactly the same when the temperature is changed? ​
Butoxors [25]

no...the atoms will not behave the same

as when temperature is increased, the atoms vibration and kinetic energy will also be increased....they come in excited state...

where as when temperature is reduced ,atoms kinetic energy slows down....

7 0
3 years ago
Describe how oxidation and reduction involve electrons, change oxidation numbers, and combine in
Sholpan [36]

Answer:

Redox

Explanation:

Reduction is gain of electrons

oxidation is loss of electrons

3 0
3 years ago
Atoms of which of the following elements are largest?<br> A:<br> Na<br> OOOO
elena-14-01-66 [18.8K]

Answer:

yes answer os Na because it's electronic configuration is 1s^2,2s^2,2p^6,3s^1

5 0
3 years ago
What volume will 2.5 mol of a gas at STP occupy ?
kvv77 [185]

Answer:

56

Explanation:

1 mole of gas at STP occupies 22.4 L of the gas

2.5 mole of the gas at STP occupies 22.4×2.5 L of the gas

so 2.5 mole of the gas at STP occupies 56 L of the gas .

6 0
3 years ago
Draw the structure(s) of the major organic product(s) of the following reaction. 1. lithium diisopropylamide / hexane 2. 1 eq. C
Jobisdone [24]

Answer:

See explanation below

Explanation:

You are not providing the starting material, however, I manage to find a similar question to this, so I'm gonna use it as a basis to help you answer yours.

Now let's analyze what is happening in the reaction so we can predict the final product.

We have a ketone here, reacting at first with LDA. This is a very strong base that is commonly used in reactions with ketones and aldehydes to promove a condensation. To do this, as LDA is a strong base it will occur firts an acid base reaction, substracting the most acidic hydrogen in the molecule (Which in this case, is the Beta hydrogen of the carbonile). This will cause an enolate formation.

Then, this enolate will react with the CH3I and form a new product. The final result would be a ketone with a methyl group now attached. In the picture 2, you have the mechanism and final product.

Hope this helps

6 0
3 years ago
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