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PSYCHO15rus [73]
3 years ago
13

I NEED HELP PLEASE!!!!!

Chemistry
2 answers:
lisov135 [29]3 years ago
7 0
Atoms can be divided more so thats not true. atoms from the same element arent all nesacarly identical because of isotopes
jolli1 [7]3 years ago
5 0
Atoms of different elements can combine physically and chemically. 
Chemical reactions occur when atoms are joined or separated.
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Answer:

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Explanation:

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Increasing the concentration of reactants generally increases the rate of a reaction because particles
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This increases the rate of rxn because the particles, because according to the Collision Theory, <span>the </span>rate of rxn <span>is proportional to number of effective collisions between the </span>reactant <span>molecules.</span>
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A technician needs 500.0mL of a 0.500 M MgCl2 solution for some lab procedures. The stock bottle is labeled 4.00 M MgCl2. What v
mihalych1998 [28]

Answer:

Explanation:

To solve this problem, we need to obtain the number of moles of the solute we desired to prepare;

    Number of moles  = molarity x volume

Parameters given;

        volume of solution = 500mL  = 0.5L

          molarity of solution = 0.5M

   Number of moles  =  0.5 x 0.5  = 0.25moles

Now to know the volume stock to take;

           Volume of stock = \frac{number of moles }{molarity}

  molarity of stock  = 4M

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4 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
Sugar dissolving in warm water is chemical or phyiscal change
BlackZzzverrR [31]
Hey there! Great question;) Answer:Physical change Explanation: When sugar mixes with water, at the end, the chemical formulas are the same. Nothing has changed! I hope this helps;)
5 0
3 years ago
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