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jolli1 [7]
2 years ago
7

The middle block of the periodic table is called?​

Chemistry
1 answer:
Masteriza [31]2 years ago
3 0

Answer: The transition metals make up the middle block of he periodic table

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If an atom has no electric charge, what can be said about the number of protons and electrons it contains?
vitfil [10]

then the electrons and protons would have a even amount of negetive electric charges

8 0
3 years ago
What's the IUPAC name pf this compound? CH3-CH-CH2-CH-CHO | | CH3 CL
Svetradugi [14.3K]

Answer:

2-chloro-4-methylpentanal.

Explanation:

Hello there!

In this case, according to the chemical compound:

CH3-CH-CH2-CH-CHO

          |              |

        CH3        Cl

We can see the main functional group is an starting carbonyl, which means this is an aldehyde. Moreover, we can see a Cl-substituent on the second carbon and a methyl substituent on the fourth carbon. Therefore, the IUPAC name turns out: 2-chloro-4-methylpentanal.

Best regards!

8 0
3 years ago
What changes in space result from the death of massive stars?
lana [24]

Whenever the fuel is being used up, a star explodes and the energy leakage from a star's core ceases.

Explanation:

The dying star expands in the "Red Giant," before even the inevitable collapse starts, due to nuclear reactions just outside of the core.

It becomes a white dwarf star when the star has almost the same density as the Sun. If it's much larger, a supernova explosion could take place and leave a neutron star away. However, if it is very large–at least three times the Sun's mass–the crumbling core of the star, nothing will ever stop it from crumbling. The star is imploding into a black hole, an endless gravitational loop in space.

6 0
3 years ago
Which of the following structures are accessory structures of the digestive system?
professor190 [17]

the pancreas and the liver

7 0
3 years ago
Read 2 more answers
Draw the major organic substitution product(s) for (2R,3S)-2-bromo-3-methylpentane reacting with the given nucleophile. Indicate
Andrew [12]

Answer:

(2R,3S)-2-ethoxy-3-methylpentane

and

(2S,3S)-2-ethoxy-3-methylpentane

Explanation:

For this case, we will have  CH_3CH_2O^- as nucleophile. Also, this compound is also in excess. So, we will have as solvent CH_3CH_2OH a protic solvent. Therefore the Sn1 reaction would be favored.

The first step would be the carbocation formation followed by the attack of the nucleophile. In this case both isomers would be produced: R and S (see figure).

7 0
2 years ago
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