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charle [14.2K]
3 years ago
5

Help me solve this equation for K please, will give brainliest

Chemistry
1 answer:
balandron [24]3 years ago
8 0

answer:

1.H²(g)+1²(g)=2H(g)

Explanation:

HAHAH IDON'T NO hahahha

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When an electron in a quantum system drops from a higher energy level to a lower one, the system __
icang [17]

When an electron in a quantum system drops from a higher energy level to a lower one, the system<u> emit a photon.</u>

<u />

The energy of the electron drops when it transitions levels, as well as the atom releases photons. The emission of the photon occurs as the electron transitions from an energy state to a lower state. The photon energy represents precisely the energy that would be lost when an electron moves to a level with less energy.

When such an excited electron transitions from one energy level to another, this could emit a photon. The energy drop would be equivalent to the power of the photon that is released. In electron volts, the energy of an electron, as well as its associated photon (emitted or absorbed) has been stated.

Therefore, when an electron in a quantum system drops from a higher energy level to a lower one, the system<u> emit a photon.</u>

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2 years ago
At STP how many moles or helium would occupy a volume of 12 liters?
butalik [34]
1 mole ------------- 22.4 L ( at STP )
?? mole ---------- 12 L

12 x 1 / 22.4 => 0.5357 moles

hope this helps! 
5 0
3 years ago
Select the keyword or phrase that will best complete each sentence.
pishuonlain [190]

Answer:

1) acetylide

2) enol

3) aldehydes

4) tautomers

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Explanation:

Acetylide anions (R-C≡C^-) is a strong nucleophile. Being a strong nucleophile, we can use it to open up an epoxide ring by SN2 mechanism. The attack of the acetylide ion occurs from the backside of the epoxide ring. It must attack at the less substituted side of the epoxide.

Oxomercuration of alkynes and hydroboration of alkynes are similar reactions in that they both yield carbonyl compounds that often exhibit keto-enol tautomerism.

The equilibrium position may lie towards the Keto form of the compound. Usually, if terminal alkynes are used, the product of the reaction is a methyl ketone.

3 0
3 years ago
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Answer:

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Explanation:

4 0
3 years ago
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Answer:

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Explanation:

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