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(a)
Interpretation:
The name of following ionic compound -
Concept Introduction:
Chemical formulas and names for ionic compounds containing polyatomic ions:
Ionic compounds containing positive and negative charges present must add to zero.
If more than one polyatomic ion is present in a compound, the chemical formula can be written as a polyatomic ion is enclose in parentheses and a subscript, placed outside of the parentheses. Example-
Sometimes same element is present in two different locations. For example,
(b)
Interpretation:
The name of following ionic compound -
Concept Introduction:
Chemical formulas and names for ionic compounds containing polyatomic ions:
Ionic compounds containing positive and negative charges present must add to zero.
If more than one polyatomic ion is present in a compound, the chemical formula can be written as a polyatomic ion is enclose in parentheses and a subscript, placed outside of the parentheses. Example-
Sometimes same element is present in two different locations. For example,
(c)
Interpretation:
The name of following ionic compound -
Concept Introduction:
Chemical formulas and names for ionic compounds containing polyatomic ions:
Ionic compounds containing positive and negative charges present must add to zero.
If more than one polyatomic ion is present in a compound, the chemical formula can be written as a polyatomic ion is enclose in parentheses and a subscript, placed outside of the parentheses. Example-
Sometimes same element is present in two different locations. For example,
(d)
Interpretation:
The name of following ionic compound -
Concept Introduction:
Chemical formulas and names for ionic compounds containing polyatomic ions:
Ionic compounds containing positive and negative charges present must add to zero.
If more than one polyatomic ion is present in a compound, the chemical formula can be written as a polyatomic ion is enclose in parentheses and a subscript, placed outside of the parentheses. Example-
Sometimes same element is present in two different locations. For example,
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Chapter 4 Solutions
EBK GENERAL, ORGANIC, AND BIOLOGICAL CH
- Label the spectrum with spectroscopyarrow_forwardLabel the spectrum with spectroscopyarrow_forwardQ1: Draw the most stable and the least stable Newman projections about the C2-C3 bond for each of the following isomers (A-C). Are the barriers to rotation identical for enantiomers A and B? How about the diastereomers (A versus C or B versus C)? enantiomers H Br H Br (S) CH3 H3C (S) (R) CH3 H3C H Br A Br H C H Br H3C (R) B (R)CH3 H Br H Br H3C (R) (S) CH3 Br H D identicalarrow_forward
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