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Kryger [21]
2 years ago
9

What is respiration explain in own words please

Chemistry
2 answers:
pashok25 [27]2 years ago
4 0

Answer: the process by which cells use oxygen to break down sugar and obtain energy.

Mrrafil [7]2 years ago
4 0

Answer:

The process in which we breathe out carbon dioxide and breathe in oxygen.

Explanation:

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Based on this information what is the most likely reason for refrigerating most foods reduce the rate at which they spoil
jasenka [17]

Answer: The lower temperature reduces molecule speeds, reducing the number of effective collisions.

Explanation:

7 0
3 years ago
How many moles are in 5.32 x 1020 atoms<br> of copper?<br> What is the answer but in numbers ?
Wewaii [24]

Answer is 1.41 x 10 with the exponent of 24, atoms

Explanation : Look at the picture i attached.

5 0
3 years ago
“Why do you think it is warmer around the equator?”
Marizza181 [45]
Because the equator is closer to the sun, the sun rays hit the earth’s surface which causes the temperature to be warm at a higher angle at the equator,
3 0
3 years ago
Read 2 more answers
Give the structure of the product obtained when cyclopropene loses a proton. Will the product be aromatic or not?
astra-53 [7]

Answer:

not aromatic

Explanation:

Cyclopropene -

as the compound is is made to lose a proton , and gains a negative charge on its ring ,

Now, The ring can become aromatic or anti - aromatic depending on the number of π electrobns ,

According to Huckel 's rule ,

The cyclic compounds with ( 4n+2 ) π electrons , where , n = 0, 1, 2, 3 ... , are considered to be aromatic in nature ,

And the cyclic compounds with ( 4n ) π electrons , where , n = 1, 2, 3 ... , are considered to be anti - aromatic in nature.

Now, for the cyclopropene structure , the number of π electron are equal to 4 , 2 from the double bond and 2 from the negative charge .

Therefore , the compound becomes not aromatic or anti - aromatic .

3 0
3 years ago
Even though the para position is one carbon farther from the carboxy group than the meta position, p-cyanobenzoic acid is more a
Nuetrik [128]

Answer:

Dissociation of O-H bond is highly favorable in p-cyanobenzoic acid resulting to higher acidity as compared to m-cyanobenzoic acid.

Explanation:

In p-cyanobenzoic acid, adjacent carbon to carboxyl group (-COOH) gets a partial positive charge due to electron withdrawing resonating effect of carboxyl group as compared to m-cyanobenzoic acid.

Due to this partial positive charge on carbon atom in p-cyanobenzoic acid, O-H bond in -COOH group remains highly polarized towards oxygen atom. Hence, dissociation of O-H bond is highly favorable in p-cyanobenzoic acid resulting to higher acidity as compared to m-cyanobenzoic acid.

Resonance structures are given below.

6 0
3 years ago
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