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AleksandrR [38]
3 years ago
6

How many single covalent bonds could an element with the electron

Chemistry
1 answer:
Tcecarenko [31]3 years ago
5 0

Answer:

1

Explanation:

I would say 1 because that configuration has 7 valence electrons.  The goal of the atom is to gain a full octet so it just needs to gain 1 more electron to get the full octet.  To get the one electron to fill the valence shell it would only need to have 1 covalent bond.

I hope this helps.  Let me know if anything is unclear.

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What is the ionic formula of the compound formed by Co3+ and the phosphorus ion? What is the name of the compound formed based o
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Answer: The ionic formula of compound is CoP and the name is cobalt phosphide.

Explanation:

For formation of a neutral ionic compound, the charges on cation and anion must be balanced. The cation is formed by loss of electrons by metals and anions are formed by gain of electrons by non metals.

Here element Co is having an oxidation state of +3 called as Co^{3+} cation and phosphprous forms P^{3-} anion with oxidation state of -3. Thus they combine and their oxidation states are exchanged and written in simplest whole number ratios to give neutral CoP

The nomenclature of ionic compounds is given by:

1. Positive is written first followed by the oxidation state of metal in roman numerals in square brackets.

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4 0
3 years ago
Which is the correct statement regarding the relative Rf values of the starting methyl benzoate vs the product, methyl m-nitrobe
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Answer:

1. The product has a higher Rf value on a silica gel TLC plate because it is more polar than the starting methyl benzoate.

2. False

3. True

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Since silica gel is a polar solvent, it will retain the more polar product methyl m-nitrobenzoate compared to the methyl benzoate starting material.

In comparing the electrophillic aromatic substitution of m-nitrobenzoate  and methyl benzoate, we must remember that the presence of electron withdrawing groups (such as -NO2 and -CHO) on the aromatic compound deactivates the compound towards electrophillic aromatic substitution hence, methyl m-nitrobenzoate is less reactive than methyl benzoate in Electrophilic Aromatic Substition and Methyl benzoate is less reactive than benzene in Electrophilic Aromatic Substition

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