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Blababa [14]
3 years ago
13

Does anyone know where i can find a practice cumulative chem test online?

Chemistry
1 answer:
Montano1993 [528]3 years ago
6 0
Exam board websites often have past papers from several previous years, if you know what exam board you are going to be using, try that, if not there may be content on the edexcel and AQA websites
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On the basis of which property of the elements are they divided into metals and non metals?
kicyunya [14]
The answer is the elements in a periodic table.  <span>On the basis of the elements in the periodic table, they are divided into metals and non metals. </span>
8 0
3 years ago
Why does the sky change colors at sunrise and sunset
aniked [119]

Answer:

As the sun's angle changes, (because of the rotation of the earth) the sun slowly begins to shine more or less sunshine slowly. When sunsets and sunrises occur, the color of the sky changes because the sunshine is starting to fade out or in.

I put it in my own words so you don't have to worry about plagiarism :)

4 0
3 years ago
Chemistry Lab Question: Filtration
tatyana61 [14]

For the first question, salt is soluble while sand is insoluble or not dissolvable in water. The salt should have vanished or melted, but the sand stayed noticeable or visible, making a dark brown solution probably with some sand particles caught on the walls of the container when the boiling water was put in to the mixture of salt and sand. The solubility of a chemical can be disturbed by temperature, and in the case of salt in water, the hot temperature of the boiling water enhanced the salt's capability to melt in it.

For the second question, the melted or dissolved salt should have easily made its way through the filter paper and into the second container, while the undissolved and muddy sand particles is caught on the filter paper. The size of the pores of the filter paper didn’t change. On the contrary, the size of the salt became smaller because it has been dissolved which is also the reason why it was able to go through the filter paper, while the size of the sand may have doubled or even tripled which made it harder to pass through.

6 0
3 years ago
After fertilization, female cones become very:<br> sticky<br> light<br> O hard
S_A_V [24]

Answer:

light

Explanation:

sorry don't now this one

8 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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