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Kisachek [45]
2 years ago
10

0.4 mole of ammonia results after 1.2 mole of nitrogen gas is combined with 1.8 mole of hydrogen gas in a 1.0 L flask. What is t

he Keq for this reaction
Chemistry
1 answer:
gavmur [86]2 years ago
4 0

Answer:

Ahhh! I had the same question

Explanation:

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In which pair would both compounds have the same empirical formula? A. H2O and H2O2 B. BaSO4 and BaSO3 C. FeO and Fe2O3 D. C6H12
Kazeer [188]
The pair of both compounds that have the same empirical formula are C6H12O6 and HC2H3O2. The answer is letter D. <span>H2O and H2O2, BaSO4 and BaSO3 and FeO and Fe2O3 do not have the same empirical formula.</span>
4 0
4 years ago
Someone help answer this for me tysm
Ghella [55]
Energy, kinetic, potential
8 0
3 years ago
Read 2 more answers
How to convert 250 in scientific notation
cricket20 [7]
In scientific notation, a number is less than ten but more than one.

Move the decimal point from 0, 250.000 <- this is the same as 250 to between 2 and 5.

I had to move two spaces.

2.5^2

I hope this helps!
~kaikers
4 0
3 years ago
What is the answer for chemestry when it says 1.204 times 10^24
Sphinxa [80]

Answer: This is called moles

Explanation:  This is described to be the number of molecules, atoms or ions in a substance :)

6 0
3 years ago
Sodium tert-butoxide (NaOC(CH3)3) is classified as bulky and acts as Bronsted Lowry base in the reaction. It is reacted with 2-c
IceJOKER [234]

Answer:but-1-ene

Explanation:This is an E2 elimination reaction .

Kindly refer the attachment for complete reaction and products.

Sodium tert-butoxide is a bulky base and hence cannot approach the substrate 2-chlorobutane from the more substituted end and hence major product formed here would not be following zaitsev rule of elimination reaction.

Sodium tert-butoxide would approach from the less hindered side that is through the primary centre and hence would lead to the formation of 1-butene .The major product formed in this reaction would be 1-butene .

As the mechanism of the reaction is E-2 so it will be a concerted mechanism and as sodium tert-butoxide will start abstracting the primary hydrogen through the less hindered side simultaneously chlorine will start leaving. As the steric repulsion in this case is less hence the transition state is relatively stabilised and leads to the formation of a kinetic product 1-butene.

Kinetic product are formed when reactions are dependent upon rate and not on thermodynamical stability.

2-butene is more thermodynamically6 stable as compared to 1-butene  

The major product formed does not follow the zaitsev rule of forming a more substituted alkene as sodium tert-butoxide cannot approach to abstract the secondary proton due to steric hindrance.

5 0
3 years ago
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