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Lynna [10]
4 years ago
11

When hydrogen is replaced by another element in a hydrocarbon, the reaction is called: addition substitution hydrogenation combu

stion
Chemistry
2 answers:
zavuch27 [327]4 years ago
8 0
Substitution.... I think.
andreyandreev [35.5K]4 years ago
7 0

Answer:substitution

Explanation:

Addition reaction is defined as the reaction in which two reactants get added to give single product.

CH_2=CH_2+H_2\rightarrow CH_3CH_3

Substitution reaction is defined as the reaction in which one atom replaces the other atom from the compound.

CH_4+Cl_2\rightarrow CH_3Cl+HCl

Hydrogenation is addition of hydrogen to unsaturated hydrocarbons.

CH_2=CH_2+H_2\xrightarrow[]{hydrogenation} CH_3CH_3

Combustion is a type of chemical reaction in which fuel is reacted with oxygen to form carbon dioxide and water.

Example:  C_6H_{12}O_6+O_2 \rightarrow CO_2+H_2O

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Pls help ill mark as brainliest :)
Alina [70]

Answer:

I think its a double reaction

Explanation:

4 0
4 years ago
In water, hydrogen bonds are best described as _____.
Elina [12.6K]

Answer: Option D) covalent bonds between water molecules

In water, hydrogen bonds are best described as covalent bonds between water molecules

Explanation:

The hydrogen bonds between water molecules are covalent bonds because they are formed when oxygen attract the lone electron in hydrogen, thus resulting in the formation of a partially negative charge on the oxygen atom and a partially positive charge on two hydrogen atoms

Thus, the sharing of electrons between oxygen and hydrogen atoms is responsible for the covalent bonds between water molecules

7 0
3 years ago
Determine the number of protons, neutrons and electrons in each of the following:
Kisachek [45]
Cu+ p=29 e=28 n=34
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I hope i did it right :))
5 0
3 years ago
H-E-L-P!!...!! ʕ ꈍᴥꈍʔ​
N76 [4]

Answer:

the correct answer is (2)

Explanation:

4 0
3 years ago
Read 2 more answers
Draw the product formed by the reaction of potassium t-butoxide with (1s,2s)-1-bromo-2-methyl-1-phenylbutane (shown below). (dra
VikaD [51]
 <span>You have to use a Newman projection to make sure that the H on C#2 is anti-coplanar with the Br on C#1. (Those are the two things that are going to be eliminated to make the alkene.) 

My Newman projection looks like this when it's in the right configuration: 
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Back carbon (C#1) has H straight down, Ph up/left, and Br up/right. 

Then when you eliminate the H from C#2 and the Br from C#1, you will have Ph and the ethyl group on the same side of the molecule, and you'll have the remaining H and CH3 on the same side of the molecule. 

This is going to give you (Z)-2-methyl-1-phenyl-1-butene.</span>
3 0
3 years ago
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