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NARA [144]
3 years ago
11

What does it mean for the energy levels in an atom to be quantized? Describe how this affects where electrons can be found

Chemistry
1 answer:
marta [7]3 years ago
3 0
When we describe the energy of a particle as quantized, we mean that only certain values of energy are allowed. ... In this case, whenever we measure the particle's energy, we will find one of those values. If the particle is measured to have 4 Joules of energy, we also know how much energy the particle can gain or lose. Quantized energy means that the electrons can possess only certain discrete energy values; values between those quantized values are not permitted
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ASAP
sammy [17]

The answer is C.

The vast difference in electronegativity of the oxygen and hydrogen in water, the O-H bond is polar.

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When two identical nonmetal atoms are bonded together the result is a?
Irina-Kira [14]
/A DIATOMIC MOLECULE
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After throwing the ball in the pool for my dog the ball sprung a leak and begin to fill with water. How many mL of water can th
ikadub [295]

Answer: i think 250ML

Explanation:

5 0
3 years ago
Mercury is a liquid meteal but it is not hard? how can we say it is a metal
NNADVOKAT [17]
What's the problem ? Hardness is not the definition of a metal. You need to expand your thinking. EVERY element is solid, liquid, and gas, over different ranges of temperature ... including all of the metals. There are only TWO elements that are liquid AT ROOM TEMPERATURE, and mercury is one of them. But on a mild day at the south pole, mercury is solid too.
7 0
3 years ago
Why is only one diastereomer formed in this reaction? Relate your answer to the mechanism you drew. b) If you used cis-stilbene
crimeas [40]

Answer:

1. Diastereomers have different physical properties (unlike most aspects of enantiomers) and often different chemical reactivity. ... Many conformational isomers are diastereomers as well. Diastereoselectivity is the preference for the formation of one or more than one diastereomer over the other in an organic reaction.

2. The result is a trans dibromide, as shown in the equation below

Explanation:

Diastereomers (sometimes called diastereoisomers) are a type of a stereoisomer.[1] Diasteoreomers are defined as non-mirror image non-identical stereoisomers. Hence, they occur when two or more stereoisomers of a compound have different configurations at one or more (but not all) of the equivalent (related) stereocenters and are not mirror images of each other.[2] When two diastereoisomers differ from each other at only one stereocenter they are epimers. Each stereocenter gives rise to two different configurations and thus typically increases the number of stereoisomers by a factor of two.

2. the addition of bromine to the trans and

cis isomers of 1,2-diphenylethene, more commonly known as trans- and cis-stilbene.

H

H

H H

trans-stilbene cis-stilbene

m.p. 122-124°C b.p. 82-84°C

density 0.970 g/mL density 1.011 g/mL

M.W. 180.25 g/mol M.W. 180.25 g/mol

In both cases, the nucleophilic double bond undergoes an electrophilic addition reaction

by the bromine reagent which proceeds via a cyclic bromonium ion. The addition of

bromine begins at one side of the double bond (either side is equally likely, but only one

option is drawn) and is followed by attack of bromide ion on the bromonium ion (again,

attack could occur at either carbon since the ion is symmetric, but only one option is

drawn). The result is a trans dibromide, as shown in the equation below:

Since the cis and trans isomers of stilbene have different geometries, it follows

that upon reaction with bromine they give rise to stereoisomeric bromonium ions and,

eventually, products that differ only by their stereochemistry.

4 0
3 years ago
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