Answer:
In atomic physics, the Bohr model or Rutherford–Bohr model, presented by Niels Bohr and Ernest Rutherford in 1913, is a system consisting of a small, dense nucleus surrounded by orbiting electrons—similar to the structure of the Solar System, but with attraction provided by electrostatic forces in place of gravity.
Answer:
3 element i.e carbon (C), hydrogen (H) and oxygen.
Explanation:
The following data were obtained from the question:
Subtance >>>>>>>> Chemical Formula
Glucose >>>>>>>>> C₆H₁₂O₆
Methane >>>>>>>> CH₄
Ethanol >>>>>>>>> C₂H₅OH
Hydrogen peroxide >> H₂O₂
From the above table, we can see that ethanol (C₂H₅OH) contains carbon (C), hydrogen (H) and oxygen
Therefore, the total number of elements present in ethanol, C₂H₅OH is 3.
1. Option A. Temperature and Salinity
2. Option D. (I think)
3. Option D.
Hope your test goes well!
The type of the bond is present Na₃PO₄ is the ionic bond. the Na₃PO₄ is the ionic compound. yes the Na₃PO₄ is the polyatomic ion.
The Na₃PO₄ is Na⁺ and PO₄³⁻. the phosphorus is the non metal and the oxygen atom is the non metal. the non meta and non meta form the covalent or molecular bond. the bond between the PO₄³⁻ bond is the covalent bond but the overall present in the Na₃PO₄ is the ionic bond . the bons in between the Na⁺ and PO₄³⁻ is the the ionic bond. the PO₄³⁻ id the polyatomic ion .
The bond between the positively charged ion and the negatively charged ion are called as the ionic bond and the compound form is the ionic compound.
To learn more about ionic bond here
brainly.com/question/29005103
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Explanation:
Ethanol can be oxidized to ethanal or acetaldehyde which is further oxidized to acid that is acetic acid.
→
[oxidation by loss of hydrogen]
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An oxidizing agent potassium dichromate(VI) solution is used to remove the hydrogen from the ethanol.
- An oxidizing agent used along with dilute sulphuric acid for acidification.
Acetaldehyde can also be reduced back to ethanol again by adding hydrogen to it by using a reducing agent that is sodium tetrahydro borate, NaBH4.
- The oxidation of aldehydes to carboxylic acids can be done by the two-step process.
- In the first step, one molecule of water is added in the presence of a catalyst that is acidic.
- There is a generation of a hydrate. (geminal 1,1-diol).
→
[reduction by the gain of electrons]
Here, the oxidizing agent used is
in the presence of acetone.