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Korolek [52]
3 years ago
9

What occurs in order to break the bond in a cl2 molecule? explanation please.

Chemistry
2 answers:
alexandr1967 [171]3 years ago
6 0

A cl2 molecule is a diatomic molecule composed of two atoms of identical halogen - chlorine. In this case, this molecule is composed of covalent bonds in which the identical atom- molecule tells that this is also non-polar. To break the bond, energy has to be absorbed to break the intermolecular force that bound the molecule together. 
ipn [44]3 years ago
3 0

Options for the question;

(1) Energy is absorbed.

(2) Energy is released.

(3) The molecule creates energy.

(4) The molecule destroys energy.

Answer:

(1) Energy is absorbed.

Explanation:

Using the Method of elimination;

Option 1 - Energy is absorbed to break bonds. Bond-breaking is an endothermic process. This means this option is correct.

Option 2 - This option is incorrect because bond breaking is endothermic in nature. Energy is being absorbed and not released.

Option 3 and 4 - These optons are wrong because energy can neither be created nor destroyed but can change from one form to another.

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SrCl2

Explanation:

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3 years ago
Both kepler's laws and newton's laws tell us something about the motion of the planets, but there are fundamental differences be
I am Lyosha [343]

Answer: See description

Explanation:

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Newton:

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Kepler's laws were mostly based on observed evidence with quantitative relationships between the mentioned variables. Newton's laws are based on calculus and symbolic equations. While Kepler's mode is basic, Newton took another step in and build a more general model for gravity (which was improved by general relativity later). In a nutshell Newton proved the scientific causes for Kepler's laws...

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
Water's ability to dissolve a wide variety of molecules is important, but more important is the hydrophobic effect, which drives
Sliva [168]

Answer:

d. Hydrophobic molecules are attracted to each other.

Explanation:

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3 years ago
What is the function of a restriction enzyme?
Advocard [28]
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Hope this helps!
5 0
3 years ago
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