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Alex73 [517]
3 years ago
6

Please Help In Chemistry

Chemistry
1 answer:
Makovka662 [10]3 years ago
5 0
Just pick 2 random nonmetals and remember your prefixes. you already have your covalent bonds. with the ionic i'm srry........
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A sample of nitrogen occupies 10.0 liters at 25°C what would be the new volume at 20°C? 7.9 L Ob 9.8 L 10.2 L 10.6 L
PtichkaEL [24]

Answer:

  9.4 liter

Explanation:

1) Data:

V₁ = 10.0 L

T₁ = 25°C = 25 + 273.15 K = 298.15 K

 P₁ = 98.7 Kpa

 T₂ = 20°C = 20 + 273.15 K = 293.15 K

  P₂ = 102.7 KPa

  V₂ = ?

2) Formula:

Used combined law of gases:

  PV / T = constant

  P₁V₁ / T₁ = P₂V₂ / T₂

3) Solution:

Solve the equation for V₂:

  V₂ = P₁V₁ T₂ / (P₂ T₁)

Substitute and compuite:

V₂ = P₁V₁ T₂ / (P₂ T₁)

V₂ = 98.7 KPa × 10.0 L × 293.15 K / (102.7 KPa × 298.15 K)

V₂ =  9.4 liter ← answer

You can learn more about gas law problems reading this other answer on

Explanation:

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The __________ system is made up of the nose, pharynx, trachea, lungs, bronchi, and alveoli. *
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Respiratory system is made of that
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Which of the following is an example of translational kinetic energy? windmill a tuning fork a person running a car parked in a
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a person running a car parked in a driveway

Explanation:

A person running a car parked in a driveway is an example of translational kinetic energy.

Translational motion is the movement of body along a straight path.

Translational kinetic energy refers to the energy of a body moving along a straight path.

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learn more:

Translational kinetic energy brainly.com/question/9924094

#learnwithBrainly

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Draw the structure(s) of the major organic product(s) of the following reaction. 1. lithium diisopropylamide / hexane 2. 1 eq. C
Jobisdone [24]

Answer:

See explanation below

Explanation:

You are not providing the starting material, however, I manage to find a similar question to this, so I'm gonna use it as a basis to help you answer yours.

Now let's analyze what is happening in the reaction so we can predict the final product.

We have a ketone here, reacting at first with LDA. This is a very strong base that is commonly used in reactions with ketones and aldehydes to promove a condensation. To do this, as LDA is a strong base it will occur firts an acid base reaction, substracting the most acidic hydrogen in the molecule (Which in this case, is the Beta hydrogen of the carbonile). This will cause an enolate formation.

Then, this enolate will react with the CH3I and form a new product. The final result would be a ketone with a methyl group now attached. In the picture 2, you have the mechanism and final product.

Hope this helps

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