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Ludmilka [50]
3 years ago
9

What is the job of a scientist?

Chemistry
2 answers:
MrMuchimi3 years ago
8 0

Answer:

c i believe, not sure

Explanation:

Ludmilka [50]3 years ago
5 0
Answer is C
Because they have to do experiments and hypothesis and do science
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Which compound has the most nonbonding electrons?
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d water I believe I'm sorry if it's wrot

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Which statement describes how technology has increased our information on Mars?
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The Curiosity rover found sulfur compounds in rocks and carbon in organic compounds like propane, butene, benzene, toluene and thiophene.

It detected methane, not in soil samples, but in the Martian atmosphere.

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Can an ion be either positive or negative? True or False
vekshin1

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True

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There is a structure of CH3CH2CHCHCH2CH3, with a –CH2CH3 group attached to the third and fourth carbons.
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2,3-diethyl hexane

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7 0
2 years ago
Give the structure of the principal organic product formed by free-radical bromination of 2,2,4−trimethylpentane.
Fudgin [204]

the principal organic product formed by free-radical bromination of 2,2,4−trimethylpentane is 2-bromo-2,4,4-trimethylpentane.

what is free radical halogenation?

A substitution reaction in which a hydrogen atom is replaced with a halogen atom, via a free radical reaction mechanism. when this reaction is carrid out by bromine radical, it is called free radicle bromination. When bromine (Br{2}) treated with light (hν) it comes to homolytic cleavage of the Br-Br bond and give rise to bromine radicles.

free-radical bromination of 2,2,4−trimethylpentane

Bromination of an alkane includes the substitution of a bromine atom for a hydrogen atom. The following stages will be taken by 2,2,4-trimethylpentane during this reaction:

Initiation reaction:  The production of a bromine free radical requires the initiation of heat or light.

Br - Br ⇒ 2Br·

Propagation: This reaction relies heavily on hydrogen. This reaction is impossible if hydrogen is not present. Because tertiary free radicals are more stable than secondary and primary free radicals, they are favoured in this reaction.

Termination: The remaining free radical of bromide reacts with the tertiary free radical of 2,2,4-trimethylpentane to form 2-bromo-2,4,4-trimethylpentane.

the principal organic product formed by free-radical bromination of 2,2,4−trimethylpentane is 2-bromo-2,4,4-trimethylpentane.

To know more about free radical halogenation, check out:

brainly.com/question/13046867

#SPJ4

7 0
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