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Naily [24]
3 years ago
8

Can somebody please help me with this question? I will appreciate it a lot !!

Chemistry
2 answers:
Alinara [238K]3 years ago
7 0
I think It would change the energy of the atom
jolli1 [7]3 years ago
5 0

Answer:

the energy of the atom

Explanation:

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Why do we use 51.0mL of NaOH but only 50.0mL of HCl?
bixtya [17]

Answer

Na OH reacts with H Cl and forms Na Cl and H₂O

NaOH + HCl   →   NaCl + H₂O                                              

Here we can see that  1 mole of NaOH reacting with 1 mole of HCl and forming 1 mole of NaCl and 1 mole of H₂O

when  NaOH and HCl are added together in equal amount then they will completely neutralize each other but NaOH is hygroscopic in nature which means it can absorb water from air so it will not be weighted accurately.

hence, for neutralization we will take extra NaOH.

3 0
3 years ago
Answer the 4 questions pls
Vedmedyk [2.9K]
A b A or just the person above me said
7 0
3 years ago
Read 2 more answers
How many molecules are in 20,484 grams of H2O?​
alexandr1967 [171]

Answer:

3.4027x10^-22

Explanation:

4 0
3 years ago
Which of the following statements is true of asexual reproduction?
katovenus [111]

Answer:

c

Explanation:

Because asexual reproduction is reproduction that requires one parent there for having only the one parents genes.

5 0
3 years ago
5.4 When looking down the C{{TOP-HAT-MATH-TOKEN-0}}-C{{TOP-HAT-MATH-TOKEN-1}} bond in 2,3-dimethylbutane, what is the most stabl
AURORKA [14]

Answer:

The most stable conformer would be the anti-conformer when the substituent methyl groups are farthest away from each other.

Explanation:

Isomers are chemical compounds with the same molecular formula but with different molecular structures.

Conformers are a special type of isomers that produce different structures when the substituents of a Carbon-Carbon single bond (C-C) are rotated.

In 2,3 dimethyl butane, the substituent methyl groups are located around the second and third Carbon to Carbon single bond.

To achieve a stable configuration, the methyl group substituents need to be as far apart as possible (that is, in an anti-position) to minimise repulsion.

The closer the methyl groups are to each other, the more they repel each other and the more unstable the conformer becomes.

7 0
3 years ago
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