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sasho [114]
3 years ago
13

Question 1 (2 points)

Chemistry
1 answer:
Anettt [7]3 years ago
4 0

Answer:

I didn't KNOW WHAT IS THE ANSWWR OF YOUR QUISTION IM SO SORRY

Explanation:

I WANT TO INTRODUCE SELF TO YOU CAN I

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In the sun, hydrogen is converted to ____________________ through nuclear fusion.
lana66690 [7]

Answer:

Helium

In the sun, hydrogen is converted to __<u>Helium</u>__ through nuclear fusion.

4 0
3 years ago
Read 2 more answers
Aluminum oxide is formed when aluminum combines with oxygen in the air. How many grams of Al2O3 are formed when 13.6 mol of Al r
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Answer:

4Al + 3O2 → 2Al2O3 a. If you use 2.3 moles of Al, how many moles of Al2O3 can ... How many grams of Al2O3 are produced from the reaction of 5 moles of Al?

Explanation:

3 0
3 years ago
The temperature at which carbon dioxide sublimes is about 195 K. What is this
Rom4ik [11]
This temperature in units of degree Celsius is..

-78° Celsius
3 0
3 years ago
Write a net ionic equation to show that acetylsalicylic acid (aspirin), hc9h7o4, behaves as a brønsted-lowry acid in water.
Thepotemich [5.8K]
By definition, Bronsted-Lowry acid is a proton donor in the acid-base neutralization reaction. When a weak acid like acetylsalicylic acid is reacted with water, the water here acts as the Bronsted-Lowry base. This is possible because water has properties of amphoterism - can act as an acid or base. In this case, acetylsalicylic acid would have to donate its H+ atom to water, so that it would yield a hydronium ion, H₃O⁺. The complete net ionic reaction is shown in the picture.

So, in the reaction, the products yield are the acetylsalicylate ion and the hydronium ion.

3 0
3 years ago
What is the major organic product obtained from the following reaction?
trapecia [35]

The correct option is (b)

NaNH2 is an effective base. It can be a good nucleophile in the few situations where its strong basicity does not have negative side effects. It is employed in elimination reactions as well as the deprotonation of weak acids.Alkynes, alcohols, and a variety of other functional groups with acidic protons, such as esters and ketones, will all be deprotonated by NaNH2, a powerful base.Alkynes are deprotonated with NaNH2 to produce what are known as "acetylide" ions. These ions are powerful nucleophiles that can react with alkyl halides to create carbon-carbon bonds and add to carbonyls in an addition reaction.Acid/base and nucleophilic substitution are the two types of reactions.Using the right base, terminal alkynes can be deprotonated to produce a carbanion.A good C is the acetylide carbanion.The acetylide carbanion can undergo nucleophilic substitution reactions because it is a potent C nucleophile. (often SN2) with 1 or 2 alkyl halides with electrophilic C to create an internal alkyne (Cl, Br, or I).Elimination is more likely to occur with 3-alkyl halides.It is possible to swap either one or both of the terminal H atoms in ethylene (acetylene) to create monosubstituted (R-C-C-H) and symmetrical (R = R') or unsymmetrical (R not equal to R') disubstituted alkynes (R-C-C-R').

Learn more about NANH2 here :-

brainly.com/question/12601787

#SPJ4

7 0
2 years ago
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