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aalyn [17]
3 years ago
14

Are formed when atoms bond together

Chemistry
1 answer:
Nadya [2.5K]3 years ago
5 0
They form chemical bonds
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Help If U Know This.....Please
skad [1K]
Question 5)

1 Hour: 100g
40 Minutes: 50g
20 Minutes: 25g
0 Minutes: 12.5g

Question 6)

160 Days: 80ou
120 Days: 40ou
80 Days: 20ou
40 Days: 10ou
0 Days: 5ou

Every period of time, the radioactive isotopes halve in numbers as they emit radiation.

I think you now know the gist. Try doing the rest yourself.

Good luck.
6 0
3 years ago
100 ml of gaseous hydrocarbon consumes 300
zhenek [66]

The answer would be a. C2H4(ethylene)

1C2H4+3O2~>2CO2+2H2O

6 0
2 years ago
Read 2 more answers
The lock-and-key mechanism refers to
miskamm [114]

Answer:

A). The complementary shapes of an enzyme and a substrate.

Explanation:

The Lock-and-key mechanism was proposed by Emil Fischer for the first time and characterized as the metaphor which helps in elucidating the specificity of the enzymatic reactions. In this metaphor, the lock is described as the enzyme while 'key' is characterized as the substrate which the enzyme acts upon. If the key is not appropriately sized, it will not fit into the active site i.e. the keyhole of the lock or enzyme and reaction will not take place. Thus, <u>option A</u> is the correct answer.

5 0
3 years ago
Read 2 more answers
Comparing the 2-bromobutane + methoxide and 2-bromobutane + t-butoxide reactions, choose the statements that BEST describe the d
Elina [12.6K]

Answer:

an increase in 1-butene was observed when t-butoxide was used

Explanation:

When a base reacts with an alkyl halide, an elimination product is formed. This reaction is an E2 reaction.

Here we are to compare the reaction of two different bases with one substrate; 2-bromobutane. Both reactions occur by the E2 mechanism but follow different transition states due to the size of the base.

The Saytzeff product, 2-butene, is obtained when the methoxide is used while the non Saytzeff product, 1-butene, is obtained when t-butoxide is used.

The Saytzeff rule is reliable in predicting the major products of simple elimination reactions of alkyl halides given the fact that a small/strong bases is used for the elimination reaction. Therefore hydroxide, methoxide and ethoxide bases give similar results for the same alkyl halide substrate. Bulky bases such as tert-butoxide tend to yield a higher percentage of the non Saytzeff product and this is usually attributed to steric hindrance.

8 0
3 years ago
Identify an alkene and carboxylic acid using primary observations
ehidna [41]

Answer:

The general formula for the carboxylic acids is C nH 2n+1COOH (where n is the number of carbon atoms in the molecule, minus 1).

Explanation:

<em>Hope </em><em>it </em><em>helps </em><em>u </em>

FOLLOW MY ACCOUNT PLS PLS

4 0
3 years ago
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