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Valentin [98]
2 years ago
5

Which metallic substance would require the least amount of thermal energy to melt?

Chemistry
2 answers:
Len [333]2 years ago
5 0

Answer: C (Aluminum)

Explanation:

Aluminum would require the least amount of thermal energy to melt, because according to the chart, it has the lowest melting point (1218ºF) as compared to the melting points of Gold (1945ºF), Nickel (2646ºF), and Steel (2500ºC).

Art [367]2 years ago
3 0
Aluminum it has the least melting point so it’s aluminum. just look and see which is the lowest number
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Gaseous dichlorine monoxide decomposes readily to chlorine (green) and oxygen (red) gases.
Stolb23 [73]

The reactants are oxygen and nitrogen monoxide.

<h3>What is nitrogen monoxide?</h3>

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To learn more about nitrogen monoxide from the given link:

brainly.com/question/13428103

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8 0
1 year ago
Someone answer these both for me
Julli [10]

Answer:

a b

Explanation:

I think so take it with a grain of salt

4 0
3 years ago
Is gasoline a compound or a mixture? compound mixture
ehidna [41]
Gasoline would be a mixture if I recalled 
3 0
3 years ago
Read 2 more answers
A solution is made by mixing 37.g of thiophene C4H4S and 72.g of heptane C7H16. Calculate the mole fraction of thiophene in this
guajiro [1.7K]

Answer:

0.38

Explanation:

Molar mass of thiophene= 84g/mol

Mass of thiophene = 37g

Number of moles= 37/84= 0.44 moles

Molar mass of heptane= 100 g/mol

Mass of heptane = 72g

Number of moles = 72/100= 0.72 moles

Total number of moles= 0.44 + 0.72= 1.16 moles

mole fraction of thiophene = 0.44/1.16= 0.38

4 0
3 years ago
The aldol reaction is catalyzed by acid as well as base. What is the reactive nucleophile in the acid-catalyzed aldol reaction
svp [43]

Answer:

The reactive nucleophile is Ketone.

Explanation:

In organic chemistry, The process of acid - catalyzed aldol condensation starts from when ketone (or any aldehyde) is converted to an -enol, after which it attacks another ketone/aldehyde that has already been activated by parbonyl oxygen protonation.

The process of this is that first of all the ketone undergoes tautomerization to form -enol. Thereafter, the other carbonyl will undergo protonation which makes the carbon activated towards attack. Now, the nucleophilic enol will be added to the carbonyl in a [1,2]-addition reaction and we will now use deprotonation to obtain the neutral Aldol product.

Now, since only the ketone can produce an -enol, thus it is the nucleophile as aldehydes are better electrophiles

4 0
3 years ago
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