
Concept explainers
Interpretation:
The table with atomic notations is to be completed by providing the missing information.
Concept introduction:
The

Answer to Problem 24E
The table with atomic notations with complete information is shown below.
Atomic Notation |
Atomic Number |
Mass Number |
Number of protons | Number of neutrons | Number of electrons |
Explanation of Solution
In the atomic notation,
The mass number can be calculated by the formula shown below.
The number of neutrons is calculated by the formula shown below.
The atomic number of the element is
Substitute the values of number of neutrons and atomic number in the equation (1).
The mass number is the element is
The mass number of the element is
Substitute the values of mass number and atomic number in the equation (2).
The number of neutrons in the element is
The atomic number of the element is
Substitute the values of number of neutrons and atomic number in the equation (1).
The mass number is of the element is
The mass number of the element is
Substitute the values of mass number and atomic number in the equation (2).
The number of neutrons in the element is
The table with the information of atomic number, mass number, number of neutrons, number of protons and number of electrons for given atomic notations is shown below.
Atomic Notation |
Atomic Number |
Mass Number |
Number of protons | Number of neutrons | Number of electrons |
The table with atomic notations with complete information is shown below.
Atomic Notation |
Atomic Number |
Mass Number |
Number of protons | Number of neutrons | Number of electrons |
Want to see more full solutions like this?
Chapter 4 Solutions
Introductory Chemistry: Concepts and Critical Thinking (8th Edition)
- Synthesize 2-Ethyl-3-methyloxirane from dimethyl(propyl)sulfonium iodide using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize 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_forward
- Synthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardIf 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_forward
- Indicate the products obtained by mixing (3-oxo-3-phenylpropyl)triphenylphosphonium bromide with sodium hydride.arrow_forwardWe 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_forward
- Indicate the products obtained by mixing 2-Propanone and ethyllithium and performing a subsequent acid hydrolysis.arrow_forwardIndicate 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_forward
- Chemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning
- General Chemistry - Standalone book (MindTap Cour...ChemistryISBN:9781305580343Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; DarrellPublisher:Cengage LearningWorld of ChemistryChemistryISBN:9780618562763Author:Steven S. ZumdahlPublisher:Houghton Mifflin College DivChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning





