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Stolb23 [73]
2 years ago
14

What is the term for the region where the north and south poles of atoms in a material will line up​

Chemistry
2 answers:
hjlf2 years ago
3 0

Answer:

ferromagnetic materials

Explanation:

neonofarm [45]2 years ago
3 0

Answer:

<u>Magnetic domains </u>are regions of matter where north and south poles of atoms line up in the same direction.

Only certain materials, called ferromagnetic materials, can be magnetized. They include iron, cobalt, and nickel.

Explanation:

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The bacteria can chemically combine nitrogen with hydrogen to form ammonia (NH3). This combining process is called nitrogen fixa
nikklg [1K]

Answer:

bacteria

Explanation:

they are decomposers. they decompose dead material by fixing nitrogen

7 0
3 years ago
Consider the following reaction:
adell [148]

Answer:

1. d[H₂O₂]/dt = -6.6 × 10⁻³ mol·L⁻¹s⁻¹; d[H₂O]/dt = 6.6 × 10⁻³ mol·L⁻¹s⁻¹

2. 0.58 mol

Explanation:

1.Given ΔO₂/Δt…

    2H₂O₂     ⟶      2H₂O     +     O₂

-½d[H₂O₂]/dt = +½d[H₂O]/dt = d[O₂]/dt  

d[H₂O₂]/dt = -2d[O₂]/dt = -2 × 3.3 × 10⁻³ mol·L⁻¹s⁻¹ = -6.6 × 10⁻³mol·L⁻¹s⁻¹

 d[H₂O]/dt =  2d[O₂]/dt =  2 × 3.3 × 10⁻³ mol·L⁻¹s⁻¹ =  6.6 × 10⁻³mol·L⁻¹s⁻¹

2. Moles of O₂  

(a) Initial moles of H₂O₂

\text{Moles} = \text{1.5 L} \times \dfrac{\text{1.0 mol}}{\text{1 L}} = \text{1.5 mol }

(b) Final moles of H₂O₂

The concentration of H₂O₂ has dropped to 0.22 mol·L⁻¹.

\text{Moles} = \text{1.5 L} \times \dfrac{\text{0.22 mol}}{\text{1 L}} = \text{0.33 mol }

(c) Moles of H₂O₂ reacted

Moles reacted = 1.5 mol - 0.33 mol = 1.17 mol

(d) Moles of O₂ formed

\text{Moles of O}_{2} = \text{1.33 mol H$_{2}$O}_{2} \times \dfrac{\text{1 mol O}_{2}}{\text{2 mol H$_{2}$O}_{2}} = \textbf{0.58 mol O}_{2}\\\\\text{The amount of oxygen formed is $\large \boxed{\textbf{0.58 mol}}$}

8 0
3 years ago
The expression 6.020 x 10^23
Montano1993 [528]

Answer:

3

Explanation:

6 0
2 years ago
Which compound matches the ir spectrum best?
Maurinko [17]
Small peak at 3000large peak at 1685F: it contains two benzene rings that is connected by a bunch of carbons and ketone-Explanation: The spectrum shows a stretching absorption consistent with a ketone functional group: carbonyl C=O stretching at ~1685 cm-1. (An aldehyde, by contrast, would also show a ~2700 cm-1 absorption for the carbonyl C-H stretch.) The C=O stretching frequency is consistent with an aromatic ketone, such as in compound F (1,4-diphenyl-1,4-butanedione). In contrast, an aliphatic ketone absorbs at higher energy (~1710 cm-1). The spectrum also shows the typical ~1600 & ~1500 cm-1 absorptions of a phenyl group.
4 0
3 years ago
Explain why, when the guanidino group of arginine is protonated, the double-bonded nitrogen is the nitrogen that accepts the pro
Jet001 [13]

Answer:

Due to the resonance structures

Explanation:

In the question:

"<em>Explain why, when the guanidino group of arginine is protonated, the double-bonded nitrogen is the nitrogen that accepts the proton. There is a scheme of a reversible reaction, where one equivalent of the reactant reacts with two equivalents of H plus</em>"

We have to take into account the structure of the <u>amino acid</u> arginine. In which, we have the amino and the carboxylic groups in the right and the <u>guanidine group in the left</u>.

In this group, we have a central carbon with three nitrogen atoms around and a double bond with the nitrogen on the top. This nitrogen on the top will accept the proton because the structure produced will have a positive charge on this nitrogen. Then, the double bond with the carbon can be delocalized into the nitrogen producing a positive charge in the carbon.

In this structure (<u>the carbocation</u>), we can have several resonance structures. In the <em>blue option</em>, we can produce a double bond with the nitrogen on the right. In the <em>purple option</em>, we can produce a double bond with the nitrogen on the left.

In conclusion, if the nitrogen in the top on the guanidine group accepts an hydrogen atom and we will have <u>several resonance structures that can stabilize the molecule.</u> Due to this, the nitrogen in the top its the best option to accept hydrogens.

See figure 1

I hope it helps!

7 0
2 years ago
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