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Debora [2.8K]
3 years ago
6

Where does heat come from

Chemistry
1 answer:
Temka [501]3 years ago
4 0

Answer:

All matter contains heat energy. Heat energy is the result of the movement of tiny particles called atoms, molecules or ions in solids, liquids and gases. Heat energy can be transferred from one object to another. The transfer or flow due to the difference in temperature between the two objects is called heat.

Explanation:

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MgCl2(at)+Br2(l)=MgBr2(at)+Cl2(g)<br><br> how do you write in a word equation
kotykmax [81]

aqueous Magnesium Chloride reacts with liquid Bromide to form aqueous Magnesium Bromide and Chlorine gas

6 0
3 years ago
can someone help me more clearly understand the difference between heterogeneous and homogeneous? Give an example of each plz.
const2013 [10]
Heterogenous mixtures are unevenly mixed. Like oil and vinegar in vinaigrette if it is not emulsified well enough and they separate. Any case where two things are not evenly distributed within each other.

Homogenous mixtures are evenly mixed throughout. Like salt water or kool-aid (when it's mixed).

Hope this helps!
3 0
3 years ago
A proton transfer reaction can occur when an aldehyde is placed in strong base, such as an alkoxide ion, producing an alcohol an
Pani-rosa [81]

Hi, you have not provided structure of the aldehyde and alkoxide ion.

Therefore i'll show a mechanism corresponding to the proton transfer by considering a simple example.

Explanation: For an example, let's consider that proton transfer is taking place between a simple aldehyde e.g. acetaldehyde and a simple alkoxide base e.g. methoxide.

The hydrogen atom attached to the carbon atom adjacent to aldehyde group are most acidic. Hence they are removed by alkoxide preferably.

After removal of proton from aldehyde, a carbanion is generated. As it is a conjugated carbanion therefore the negative charge on carbon atom can conjugate through the carbonyl group to form an enolate which is another canonical form of the carbanion.

All the structures are shown below.

7 0
3 years ago
What would be the major product obtained from hydroboration–oxidation of the following alkenes?
zmey [24]

Answer:

a. 3-methylbutan-2-ol

b. 2-methylcyclohexan-1-ol

Explanation:

For this reaction, we must remember that the hydroboration is an <u>"anti-Markovnikov" reaction</u>. This means that the "OH" will be added at the <em>least substituted carbon of the double bond.</em>

In the case of <u>2-methyl-2-butene</u>, the double bond is between carbons 2 and 3. Carbon 2 has two bonds with two methyls and carbon 3 is attached to 1 carbon. Therefore <u>the "OH" will be added to carbon three</u> producing <u>3-methylbutan-2-ol</u>.

For 1-methylcyclohexene, the double bond is between carbons 1 and 2. Carbon 1 is attached to two carbons (carbons 6 and 7) and carbon 2 is attached to one carbon (carbon 3). Therefore<u> the "OH" will be added to carbon 2</u> producing <u>2-methylcyclohexan-1-ol</u>.

See figure 1

I hope it helps!

8 0
3 years ago
Whats the name?!?!?!??!?!?!?!?!?!?!!?!?!?!??!?!?!?!
SIZIF [17.4K]
Hydrogen i suppose is the right one
7 0
3 years ago
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