Interpretation:
The names of the given compounds are to be identified from the formula.
Concept introduction:
Steps for naming the ionic compounds are as follows:
Identify the cation and the anion in the compound.
Combine the names of the cations and the anions by elimination of the word ‘ion’ from the names of the individual ions.
For metals that shows more than one charge on them, distinction is made according to the roman numerals indicated against their name.
Oxo-anions are those ions that contains one or more oxygen atoms bonded to one central atom of another element.
The oxoacids are named according to the names of the oxoanions from which they are derived. The acid based on an -ate ion is called –ic acid.

Answer to Problem 62QP
Solution:
a)
Potassium hypochlorite
b)
Silver carbonate
c)
Nitrous acid
d)
Potassium permanganate
e)
Cesium chlorate
f)
Potassium ammonium sulfate
g)
Iron
h)
Iron
i)
Titanium
j)
Sodium hydride
k)
Lithium nitride
l)
Sodium oxide
m)
Sodium peroxide
Explanation of Solution
a)
The compound
of
b)
The compound
c)
The compound
d)
The compound
e)
The compound
f)
The compound
g)
The compound
h)
The compound
i)
The compound
j)
The compound
k)
The compound
l)
The compound
m)
The compound
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Chapter 2 Solutions
BURDGE CHEMISTRY VALUE ED (LL)
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- What does the phrase 'fit for purpose' mean in relation to analytical chemistry? Please provide examples too.arrow_forwardFor each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects Resonance Effects Overall Electron-Density × NO2 ○ donating O donating O withdrawing O withdrawing O electron-rich electron-deficient no inductive effects O no resonance effects O similar to benzene E [ CI O donating withdrawing O no inductive effects Explanation Check ○ donating withdrawing no resonance effects electron-rich electron-deficient O similar to benzene © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center Accesarrow_forwardUnderstanding how substituents activate Rank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. Explanation HN NH2 Check X (Choose one) (Choose one) (Choose one) (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center Aarrow_forward
- Identifying electron-donating and electron-withdrawing effects on benzene For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Inductive Effects Resonance Effects Overall Electron-Density Molecule CF3 O donating O donating O withdrawing O withdrawing O no inductive effects O no resonance effects electron-rich electron-deficient O similar to benzene CH3 O donating O withdrawing O no inductive effects O donating O withdrawing Ono resonance effects O electron-rich O electron-deficient O similar to benzene Explanation Check Х © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forward* Hint: Think back to Chem 1 solubility rules. Follow Up Questions for Part B 12. What impact do the following disturbances to a system at equilibrium have on k, the rate constant for the forward reaction? Explain. (4 pts) a) Changing the concentration of a reactant or product. (2 pts) b) Changing the temperature of an exothermic reaction. (2 pts) ofarrow_forwardDraw TWO general chemical equation to prepare Symmetrical and non-Symmetrical ethers Draw 1 chemical reaction of an etherarrow_forward
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