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ch4aika [34]
3 years ago
15

What two kinds of energy are associated with flames

Chemistry
1 answer:
Vaselesa [24]3 years ago
3 0

Answer:

heat energy and chemical energy i believe?

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As ice melts from a solid to a liquid, A) entropy increase
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That answer is false 
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Which of the following would be more likely to conduct electrons? Strontium or Iodine? Defend your choice.
Alchen [17]
Strontium because it is a metal
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How many moles of gas are in 4.4 mL at 1.2 atm?
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The Correct Answer Is 3.2
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2 years ago
Would it be C..? <br> More NO2 and SO2 would form..help..please and thank you
Scorpion4ik [409]

Answer:

C. More NO2 and SO2 will form

Explanation:

Le Chatelier's Principle : It  predicts the behavior of equilibrium due to change in pressure , temperature , volume , concentration etc

It states that When external changes are introduced in the equilibrium then it will shift the equilibrium in a direction to reduce the change.

In given Reaction SO3 is introduced(increased) .

So equilibrium will shift in the direction where SO3 should be consumed(decreased)

Hence the equilibrium will go in backward direction , i.e

NO + SO_{3} \rightarrow NO_{2} + SO_{2}

So more and more Of NO2 and SO2 will form

7 0
3 years ago
In a two-step synthesis, C6H11Br is converted into C6H12O. From the structure of the product, molecular formula of the starting
tamaranim1 [39]

Answer:

See explanation below

Explanation:

The question is incomplete. However in picture 1, you have the starting materials and the structure of the product, which you miss in this part.

Now, in picture 2, you have the starting reactant and the product, and the mechanism that is taking place here.

First, all what we have here is an acid  base reaction. In the first step, we are using the acid medium to convert the reactant into an alcohol. The bromine there, is not leaving the molecule yet, because it's neccesary for the next step. The starting reactant is an alkene, in that way, we can convert the reactant in the first step into a secondary alcohol. In other words, the first reaction is a alkene hydration.

In the second step, we use a strong base. You may say this is a strong nucleophile and will do a Sn2 reaction to form another alcohol there, but it's not the case, because, before any kind of reaction happens, the priority here is always the acid base, so the base will react with the acidic hydrogen. In this case, it will substract an hydrogen from the OH. When this happens, the lone pair will do an auto condensation here, and attacks the bromine in the molecule. In this way, the molecule will become a cyclomolecule, and that way it form the final product.

See picture 2, for mechanism

8 0
3 years ago
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