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drek231 [11]
3 years ago
10

I need helpppp plzzzz

Chemistry
1 answer:
Inessa [10]3 years ago
8 0

Answer:

at first i would like to tell which class

Explanation:

125000 is the answwr

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Which answer is a scientifically accurate description of velocity?
agasfer [191]

Answer:

B. The motorcyclist traveled southeast along a highway at 55 mph and reached the campsite in less than the two-hour estimated time.

Explanation:

<em>Velocity </em>is the rate at which an object changes position in a specific direction. It has both <em>magnitude and direction.</em>

Travelling <em>southeast</em> at <em>55 mph</em> is a <em>velocity</em>. It gives both speed and direction.

Statements A., B., and C. give the direction but not the speed.

3 0
3 years ago
Read 2 more answers
♡
Oksi-84 [34.3K]

Your question has been heard loud and clear.

Both scientific laws and scientific theories are not based on hypothesis.

Because , scientific laws are proven and so they are real not hypothetical.

Whereas scientifc theories can be hypothetical.

Thank you

4 0
3 years ago
A ball has a mass of 0.5g and a volume of 10mL. Calculate the density
icang [17]

Answer:

0.05g/ml

Explanation:

density is equal to mass over volume check pic for more info

6 0
3 years ago
Assume an object A with a mass of 66.789 g and a volume of 10.1 mL. what is its density?
docker41 [41]

Answer: 6.61

Explanation:

5 0
3 years ago
Which is the correct statement regarding the relative Rf values of the starting methyl benzoate vs the product, methyl m-nitrobe
Marianna [84]

Answer:

1. The product has a higher Rf value on a silica gel TLC plate because it is more polar than the starting methyl benzoate.

2. False

3. True

Explanation:

In chromatography, there is a stationary phase and a mobile phase. The ratio of the distance moved by a component and the distance moved by the solvent gives the retention factor (Rf).

Since silica gel is a polar solvent, it will retain the more polar product methyl m-nitrobenzoate compared to the methyl benzoate starting material.

In comparing the electrophillic aromatic substitution of m-nitrobenzoate  and methyl benzoate, we must remember that the presence of electron withdrawing groups (such as -NO2 and -CHO) on the aromatic compound deactivates the compound towards electrophillic aromatic substitution hence, methyl m-nitrobenzoate is less reactive than methyl benzoate in Electrophilic Aromatic Substition and Methyl benzoate is less reactive than benzene in Electrophilic Aromatic Substition

5 0
3 years ago
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