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EastWind [94]
2 years ago
5

Which of these is a Physical Change?

Chemistry
1 answer:
notka56 [123]2 years ago
5 0
D. Baking cookies I hope that’s right
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What mass in grams of nitric acid is required to react with 750 g C7H8?
lara31 [8.8K]

Answer:

932.27 i think

Explanation:

5 0
3 years ago
How many atoms are in 1 mole of hydrogen
Angelina_Jolie [31]
There are TWO atoms in one molecule of hydrogen.
8 0
2 years ago
How many calories are absorbed in a process that absorbs 0.128 joules?
earnstyle [38]

Answer:

There are 0.0305 calories in 0.128 joules

Explanation:

Given that,

Heat absorbed, Q = 0.128 J

We need to find the heat energy absorbed in calories.

We know that the relation between joules and calories is as follows :

1 calorie = 4.184 J

1 J = (1/4.184) J

So,

0.128\ J=\dfrac{0.128 }{4.184}\\\\=0.0305\ cal

So, there are 0.0305 calories in 0.128 joules

7 0
2 years ago
How many ml of a 2.0 m nabr solution are needed to make 200.0 ml of 0.50 m nabr?
gogolik [260]

To solve this we use the equation,

 

<span> M1V1 = M2V2</span>

 

<span> where M1 is the concentration of the stock solution, V1 is the volume of the stock solution, M2 is the concentration of the new solution and V2 is its volume.</span>

 

<span>2.0 M x V1 = 0.50 M x 200 mL</span>

<span>V1 = 50 mL needed</span>

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
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