
Concept explainers
(a)
Interpretation:
The maximum positive oxidation state of
(a)

Explanation of Solution
The number of electron loosed or gained in the formation if molecule is known as oxidation state or number.
The general electronic configuration of
After removal of 4 electrons it is become,
Not able to remove more electrons from
(b)
Interpretation:
The maximum positive oxidation state of
(b)

Explanation of Solution
The number of electron loosed or gained in the formation if molecule is known as oxidation state or number.
The general electronic configuration of
After removal of 6 electrons it is become,
Not able to remove more electrons from
(c)
Interpretation:
The maximum positive oxidation state of
(c)

Explanation of Solution
The number of electron loosed or gained in the formation if molecule is known as oxidation state or number.
The general electronic configuration of
After removal of 5 electrons it is become,
Not able to remove more electrons from
(d)
Interpretation:
The maximum positive oxidation state of
(d)

Explanation of Solution
The number of electron loosed or gained in the formation if molecule is known as oxidation state or number.
The general electronic configuration of
After removal of 7 electrons it is become,
Not able to remove more electrons from
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Chapter 19 Solutions
Chemistry: Principles and Practice
- Synthesize 2-Hydroxy-2-phenylacetonitrile from phenylmethanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forward
- If possible, please provide the formula of the compound 3,3-dimethylbut-2-enal.arrow_forwardSynthesize 1,4-dibromobenzene from acetanilide (N-phenylacetamide) using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardIndicate the products obtained by mixing (3-oxo-3-phenylpropyl)triphenylphosphonium bromide with sodium hydride.arrow_forward
- We mix N-ethyl-2-hexanamine with excess methyl iodide and followed by heating with aqueous Ag2O. Indicate the major products obtained.arrow_forwardIndicate the products obtained by mixing acetophenone with iodine and NaOH.arrow_forwardIndicate the products obtained by mixing 2-Propanone and ethyllithium and performing a subsequent acid hydrolysis.arrow_forward
- Indicate the products obtained if (E)-2-butenal and 3-oxo-butanenitrile are mixed with sodium ethoxide in ethanol.arrow_forwardQuestion 3 (4 points), Draw a full arrow-pushing mechanism for the following reaction Please draw all structures clearly. Note that this intramolecular cyclization is analogous to the mechanism for halohydrin formation. COH Br + HBr Brarrow_forwardIndicate the products obtained if 2,2-dimethylpropanal and acetaldehyde are mixed with sodium ethoxide in ethanol.arrow_forward
- Principles of Modern ChemistryChemistryISBN:9781305079113Author:David W. Oxtoby, H. Pat Gillis, Laurie J. ButlerPublisher:Cengage Learning
