Concept explainers
Interpretation:
Given table has to be filled with the respective values or formulas.

Explanation of Solution
Entry 1:
Name is given as phosphorus. The formula of phosphorus is
Entry 2:
Formula of the compound is given as
Therefore, oxidation state of phosphorus in ammonium hydrogen phosphate is
Entry 3:
Name is given as Phosphoric acid. The formula of Phosphoric acid is
Therefore, oxidation state of phosphorus in phosphoric acid is
Entry 4:
Name is given as Tetraphosphorus decaoxide. The formula of Tetraphosphorus decaoxide is
Therefore, oxidation state of phosphorus in Tetraphosphorus decaoxide is
Entry 5:
Formula of the compound is given as
Therefore, oxidation state of phosphorus in
Entry 6:
Name is given as calcium dihydrogen phosphate. The formula of calcium dihydrogen phosphate is
Therefore, oxidation state of phosphorus in calcium dihydrogen phosphate is
The complete table can be given as,
Formula | Name | Oxidation state of phosphorus |
Phosphorus | Zero | |
Ammonium hydrogen phosphate | ||
Phosphoric acid | ||
Tetraphosphorus decaoxide | ||
Calcium phosphate | ||
calcium dihydrogen phosphate |
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Chapter 19 Solutions
OWLv2 for Moore/Stanitski's Chemistry: The Molecular Science, 5th Edition, [Instant Access], 1 term (6 months)
- Q2: Explain why epoxides that react in an SN1 manner will not show any stereochemical inversion in the product. Q3: Rationalize why Alcohol B will react under the indicated reaction conditions, but Alcohol A will not. A ☑ OH B OH PBr3 R-Brarrow_forwardQ1: Predict the major organic product(s) of the following reactions. Include stereochemistry when necessary. Write NR if no reaction, try to explain. 1.) LDA, THF 2.) СОН CI OH H2SO4, heat OH m...... OH 1.) PCC, CH2Cl2 2.) CH3CH2MgBr, THF 3.) H3O+ 4.) TsCl, pyr 5.) tBuOK, tBuOH 1.) SOCI 2, CHCI 3 2.) CH3CH2ONA, DMF OH 1.) HBr 2.) Mg, THF 3.) H₂CO, THE 4.) H3O+ OH NaH, THFarrow_forwardWhat is the stepwise mechanism for this reaction?arrow_forward
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- Predict the organic product of Y that is formed in the reaction below, and draw the skeletal ("line") structures of the missing organic product. Please include all steps & drawings & explanations.arrow_forwardPlease choose the best reagents to complete the following reactionarrow_forwardProblem 6-17 Look at the following energy diagram: Energy Reaction progress (a) Is AG for the reaction positive or negative? Label it on the diagram. (b) How many steps are involved in the reaction? (c) How many transition states are there? Label them on the diagram. Problem 6-19 What is the difference between a transition state and an intermediate? Problem 6-21 Draw an energy diagram for a two-step reaction with Keq > 1. Label the overall AG°, transition states, and intermediate. Is AG° positive or negative? Problem 6-23 Draw an energy diagram for a reaction with Keq = 1. What is the value of AG° in this reaction?arrow_forward
- Problem 6-37 Draw the different monochlorinated constitutional isomers you would obtain by the radical chlorination of the following compounds. (b) (c) Problem 6-39 Show the structure of the carbocation that would result when each of the following alkenes reacts with an acid, H+. (a) (b) (c)arrow_forwardPlease draw the major product of this reaction. Ignore inorganic byproducts and the carboxylic side productarrow_forwardPlease draw the major product of this reaction.arrow_forward
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningChemistry for Engineering StudentsChemistryISBN:9781337398909Author:Lawrence S. Brown, Tom HolmePublisher:Cengage Learning


