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N76 [4]
4 years ago
14

Samantha is using a lever to lift a rock. To life the rock most easily, where should she apply force to the lever

Chemistry
1 answer:
Inessa [10]4 years ago
6 0

Answer:

On the opposite side of the rock.

Explanation:

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A relationship between two organisms that benefits both organisms is called
Alex777 [14]

Answer:

Mutualism

Explanation:

A relationship in which both benefit

3 0
3 years ago
Thermochromic ink, for which new uses are appearing in the fashion industry, is able to do what?
neonofarm [45]
<span>Thermochromic ink is a  kind of material that takes advantage of thermochromism. In chemistry, this is where a substance changes hues when exposed varying kinds of temperature. In the fashion industry, these inks are used for creating different kinds of accessories, clothing and bag designs. </span>
6 0
3 years ago
What would be the total volume of the new solution when it is changed from 0.2 M to 0.04 M?
34kurt
The question is incomplete.

You need two additional data:

1) the original volume
2) what solution you added to change the volume.

This is a molarity problem, so remember molarity definition and formula:

M = n / V in liters: number of moles per liter of solution

To give you the key to answer this kind of questions, supppose the original volumen was 1 ml and that you added only water (solvent).

The original solution was:

V= 1 ml
M = 0.2 M

Using the formula for molarity, M = n / V

n = M×V = 0.2 M × (1 / 10000)l = 0.0002 moles

For the final solution:

n = 0.0002 moles
M = 0.04

From M = n / V ⇒ V = n / M = 0.002 moles / 0.04 M = 0.05 l

Change to ml ⇒ 0.05 l × 1000 ml / l = 50 ml.  This would be the answer for the hypothetical problem that I assumed for you.

I hope this gives you all the cues you need to answer similar problems about molarity.
6 0
3 years ago
Read 2 more answers
1. Any gentle wind is called a
liubo4ka [24]

It's called a breeze

5 0
3 years ago
Read 2 more answers
Show the mechanism for the following reaction conducted at –5 °C in CCl4: cyclohexene bromine yields a dibromocyclohexane Draw w
Darya [45]

Answer:

See attachment.

Explanation:

In the first step, a cyclic structure with a positive bromine is formed. The bromine shares the positive charge with the two carbons that it is bonded to, so the carbons are partially positive.

The second bromine atom then attacks the carbon center, coming in from below the first bromine atom ("backside attack") where the antibonding orbital of the second bromine atom is.

The stereochemistry of the mechanism causes the final product to be an anti-dibromocyclohexane.

7 0
3 years ago
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