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Nat2105 [25]
3 years ago
11

Which solution can turn phenolphthalein pink?

Chemistry
1 answer:
Rasek [7]3 years ago
3 0
I’m pretty sure it’s A sorry if wrong
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PLS HELPPPP
Nady [450]

Answer:

1. First one is true : as per periodic table down the group , the elements has increasing order of shell & with that the London dispersion forces brings the inter-molecules close together and bromine converted into liquid .

2. second one is False  because carbon-carbon bonds are not weak bonds they form mutual covalent bonds which are stronger bonds and cannot be easily disrupted .

3. A single carbon atom has the valency of 4 so it can be bonded with four hydrogen atom at the same time .

Explanation:

5 0
3 years ago
For the procedural error, indicate if the error will affect the actual yield of copper(II) saccharinate product and if it does,
jolli1 [7]

Answer:

Lowers the actual yield

Explanation:

5 0
3 years ago
Which of the following are the requirements when creating a hypothesis for an experiment? Check ALL that apply. A: A hypothesis
kkurt [141]

Answer:

You're answer would be B.

Explanation:

5 0
3 years ago
Read 2 more answers
16.6g CaCl2 dissolved in water and completely dissociates. The molality of chloride ions in 300g of water is
vova2212 [387]

Answer:

— The molality of chloride ions in 300g of water is. A) 1.00 molal. B) 0.500 molal. C) 0.0553 molal. D) 0.111 molal.

3 0
2 years ago
Sighting along the C2-C3 bond of 2-methylbutane, the least stable conformation (Newman projection) has a total energy strain of
natima [27]

Answer:

21 KJ/mol

Explanation:

For this question, we have to start with the <u>linear structure</u> of 2-methylbutane. With the linear structure, we can start to propose all the <u>Newman projections</u> keep it in mind that the point of view is between carbons 2 and 3 (see figure 1).

Additionally, we have several <u>energy values for each interaction</u> present in the Newman structures:

-) Methyl-methyl <em>gauche: 3.8 KJ/mol</em>

-) Methyl-H <em>eclipse: 6.0 KJ/mol</em>

-) Methyl-methyl <em>eclipse: 11.0 KJ/mol</em>

-) H-H <em>eclipse:</em> 4.0 KJ/mol

Now, we can calculate the energy for each molecule.

<u>Molecule A</u>

In this molecule, we have 2 Methyl-methyl <em>gauche </em>interactions only, so:

(3.8x2) = 7.6 KJ/mol

<u>Molecule B</u>

In this molecule, we have a Methyl-methyl <em>eclipse </em>interaction a Methyl-H <em>eclipse </em>interaction and an H-H <em>eclipse</em> interaction, so:

(11)+(6)+(4) = 21 KJ/mol

<u>Molecule C</u>

In this molecule, we have 1 Methyl-methyl <em>gauche </em>interaction only, so:

3.8 KJ/mol

<u>Molecule D</u>

In this molecule, we have three Methyl-H <em>eclipse </em>interaction, so:

(6*3) = 18 KJ/mol

<u>Molecule E</u>

In this molecule, we have 1 Methyl-methyl <em>gauche </em>interaction only, so:

3.8 KJ/mol

<u>Molecule F</u>

In this molecule, we have a Methyl-methyl <em>eclipse </em>interaction a Methyl-H <em>eclipse </em>interaction and an H-H <em>eclipse</em> interaction, so:

(11)+(6)+(4) = 21 KJ/mol

The structures with higher energies would be less stable. In this case, structures B and F with an energy value of 21 KJ/mol (see figure 2).

I hope it helps!

3 0
3 years ago
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