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OleMash [197]
3 years ago
9

What is the most poisonous animal?

Chemistry
1 answer:
astraxan [27]3 years ago
5 0

Answer:

That depends on what species it is

Explanation:

Like reptiles it is rattlesnakes

Spiders would be black widow

So it depends on the what species you what.

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Which statement does NOT apply to Alkenes?
nikdorinn [45]

Answer:

They are more stable than alkanes

Explanation:

  • <em><u>Alkenes</u></em><em><u> are a type of unsaturated hydrocarbons </u></em>which means they have a<u> double bond</u> in their structure, or lack maximum number of hydrogen atoms on each carbon.
  • Alkenes have a general formula of CnH2n. They are called <u>unsaturated hydrocarbons</u> since they have a double bond. They are therefore less stable compared to alkanes and also are readily reactive.
6 0
3 years ago
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Why do you think most lampshades are made of translucent materials instead of transparent materials?
Gala2k [10]

Explanation:

because translucent shades lets the light through easily (gentle diffusion)

6 0
2 years ago
Which force is most responsible for binding together an atom’s protons and neutrons?
vampirchik [111]

Answer:

Hello There!!

Explanation:

I believe the answer is nuclear.

hope this helps,have a great day!!

~Pinky~

3 0
2 years ago
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The nucleus contains positively charged ___ and neutral ___ and makes up more than 99% of the mass of an atom.
Mashcka [7]

Answer:

ions

Explanation:

atoms because of the charge

5 0
3 years ago
the following reaction gives a product with the molecular formula c4h8o2. draw the structure of the product.
grandymaker [24]

The following reaction gives a product with the molecular formula C₄H₈O₂. The diagram of the structure of the product can be seen in the image attached below.

The reaction between C₂H₂(ONa)₂ and C₂H₄Br results in the formation of the product C₄H₈O₂ and 2NaBr.

This reaction undergoes an SN₂ mechanism since there is no stable carbocation formed. In the reaction -O⁻Na⁺ attacks the ortho position in C₂H₄Br to form C₄H₈O₂.

In  SN₂ mechanism is a nucleophilic substitution reaction where one bond is formed while another one is broken simultaneously.

The mechanism for the reaction can be seen in the image attached below.

Learn more about nucleophilic substitution reaction here:

brainly.com/question/4699407?referrer=searchResults

7 0
3 years ago
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