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goldfiish [28.3K]
3 years ago
12

A substance that conducts electricity, is malleable, ductile, and has luster would be classified as a A) compound B) element C)

metal D) nonmetal
Chemistry
2 answers:
IgorLugansk [536]3 years ago
6 0

Answer: Option (C) is the correct answer.

Explanation:

The properties of a metal are as follows.

  • Metals are malleable that is they can be drawn into thin sheets.
  • They have luster.
  • They are good conductor of electricity.
  • They are ductile that is metals can be drawn into wires.

Thus, we can conclude that a substance that conducts electricity, is malleable, ductile, and has luster would be classified as a metal.

Sati [7]3 years ago
5 0
C. Metal

You can think of aluminum cans foils
They are both malleable (to morph easily)
They both are ductile (to flatten out)
They both have luster (shiny)
And they both conduct electricity.
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Determine the moles of NH3 that can form from 70.0 grams N2.
Darina [25.2K]

Hey there!

5 moles will be produced.

N₂ has a molar mass of 28.014 g/mol.

Convert 70g to mol:

70 ÷ 28.014 = 2.5

In N₂ there are 2 nitrogen atoms. In NH₃ there is 1 nitrogen atom.

So, there will be twice as many moles of NH₃ because every one molecule of N₂ will produce two molecules of NH₃.

2.5 x 2 = 5 moles

Hope this helps!

4 0
3 years ago
Formula los siguientes compuesto: Dietil eter, Etanol, Propanotriol, Acido Propanodioico, Pentanal, Pentano-2,4-diona, Metanoato
9966 [12]

Answer:

Explanation:

En este caso para formular los compuestos, debes identificar el grupo funcional principal de la molecula. Una vez que eso está hecho, puedes intentar formularlo.

Empezaremos primero identificando el grupo funcional principal de la molécula, para luego formularlo correctamente.

Dietil eter: la terminación eter al final significa que pertenece al grupo de los éteres, el cual tiene como formula general R - O - R.

Etanol: debido a que termina en ol, este grupo pertenece a los alcoholes. Para formularlo solo se dibuja la molecula del etano, junto a un enlace con el grupo OH, como su formula general R - OH.

Propanotriol: igualmente termina en ol, por lo tanto es un alcohol, sin embargo, en este caso, tambien tiene la terminación prefija tri, asi que significa que hay 3 grupos OH en la molecula.

Acido propanodioico: esta es sencilla, porque empieza como acido, y solo hay un grupo funcional que empieza así y son los acidos carboxilicos, es decir, el grupo COOH (R - COOH) que es el carboxilo. Tiene el prefijo di, antes del oico, por lo que son dos carboxilos presentes en la molecula.

Pentanal: el sufijo al, significa que pertenece al grupo de los aldehidos, en este caso, posee el grupo carbonilo H - C = O.

Pentano - 2,4 - diona: la terminación ona significa que pertenece al grupo de las cetonas, (R - CO - R), parecido a los aldehidos, con la diferencia de que tiene grupos alquilos en lugar de un hidrogeno.

Metanoato de metilo: la terminación ato de ilo, pertenece a los esteres, (R - COOR) derivado de los acidos carboxilicos.

De aqui en adelante solo mencionaré los grupos funcionales pues ya se explicó el por que, por sus terminaciones:

Ciclohexano - 1.3 - diol: este pertenece a los alcoholes.

Acido heptanoico: acido carboxilico

Ciclobutil metil eter: eteres

Acetato de etilo: ester

2-metilbenzaldehído: aldehído unido a un grupo aromatico como el benceno.

Ciclohexanona: un ciclo (cadena cerrada) unido a un grupo carbonilo.

Butanona: cetona.

Observa la foto adjunta para que veas la formulación de cada una:

5 0
3 years ago
If you take a 15.0-mL portion of the stock solution and dilute it to a total volume of 0.600 L , what will be the concentration
alexira [117]

15 \div .6
6 0
3 years ago
1. Draw a wedge/dash structure for trans-1,2-dimethylcyclohexane.
Angelina_Jolie [31]

Answer:

The structure with the ring flipped is the most stable

Explanation:

We have the  trans 1,2 - dimethylcyclohexane. With the wedge/dash structure we could not figure is this form is stable (If we do a comparison with the cis structure). But when we do a chair structure and ring flipped structure, this is easier to look.

The picture attached shows the structures, they are labeled as 1, 2 and 3, according to this problem.

In the chair structure, according to the picture below, you can see that both methyls are heading in the axial positions of the ring (One facing upward and the other downward). This is pretty stable, however, when the methyls are in those positions, the methyl position 1, can undergoes an 1,3 diaxial interactions with the hydrogens atoms (They are not drawn, but still are there), so this interaction makes this structure a little less stable that it can be.

On the other side, the ring flipped structure, we can see that both methyls are in the equatorials positions of the ring, and in these positions, it can avoid the 1,4 diaxial interactions with the hydrogens atoms, making this structure the most stable structure.

Hope this helps

6 0
3 years ago
Sheela wants to make a computer model of a land ecosystem. Part of her model simulates the chemical processes of photosynthesis
shusha [124]
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5 0
3 years ago
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