Living by Chemistry
2nd Edition
ISBN: 9781464142314
Author: Angelica M. Stacy
Publisher: W. H. Freeman
expand_more
expand_more
format_list_bulleted
Question
Chapter U1.22, Problem 3E
Interpretation Introduction
Interpretation:
The name of the ionic compounds needs to be determined.
Concept introduction:
Some ionic species are composed of more than one atom. These are called polyatomic ions. The entire cluster of atoms shares the charge on a polyatomic ion. Each polyatomic ion has a charge that is used when writing formulae of the compound.
Expert Solution & Answer
Answer to Problem 3E
The following table shows names of ionic compounds.
| Formulae | Name of compounds |
| a. NH4Cl | Ammonium chloride |
| K2SO4 | Potassium sulfate |
| c. Al(OH)3 | Aluminium hydroxide |
| d. MgCO3 | Magnesium carbonate |
Explanation of Solution
Given information:
Formulae of some ionic compounds are given.
| Formulae |
| a. NH4Cl |
| b. K2SO4 |
| c. Al(OH)3 |
| d. MgCO3 |
Each polyatomic ion has a unique name that is used while naming the compound. Ionic compounds with polyatomic ions follow certain naming rules. Each polyatomic ion has its own name such as hydroxide for (OH-), nitrate for (NO3-), carbonate for (CO32-), sulfate for (SO42-) etc. While naming the compounds, the polyatomic ion name is added either in the beginning or end of the chemical name. Cation is named first and then anion.
- NH4Cl - Here ammonium (NH4 + ) is the polyatomic cation. So the compound is named as ammonium chloride.
- K2SO4 - Here sulfate (SO42-) is the polyatomic anion. So the compound is named as potassium sulfate.
- Al(OH)3 - Here hydroxide (OH-) is the polyatomic anion. So the compound is named as aluminium hydroxide.
- MgCO3 - Here carbonate (CO32-) is the polyatomic anion. So the compound is named as magnesium carbonate.
Conclusion
Ionic compounds with polyatomic ions follow certain naming rules. Polyatomic ions are a group of atoms bonded together.
Chapter U1 Solutions
Living by Chemistry
Ch. U1.1 - Prob. 1TAICh. U1.1 - Prob. 1ECh. U1.1 - Prob. 2ECh. U1.1 - Prob. 3ECh. U1.1 - Prob. 4ECh. U1.1 - Prob. 5ECh. U1.1 - Prob. 6ECh. U1.1 - Prob. 7ECh. U1.1 - Prob. 8ECh. U1.2 - Prob. 1TAI
Ch. U1.2 - Prob. 1ECh. U1.2 - Prob. 2ECh. U1.2 - Prob. 5ECh. U1.3 - Prob. 1TAICh. U1.3 - Prob. 1ECh. U1.3 - Prob. 2ECh. U1.3 - Prob. 3ECh. U1.3 - Prob. 4ECh. U1.3 - Prob. 5ECh. U1.3 - Prob. 6ECh. U1.4 - Prob. 1TAICh. U1.4 - Prob. 1ECh. U1.4 - Prob. 2ECh. U1.4 - Prob. 3ECh. U1.4 - Prob. 4ECh. U1.4 - Prob. 5ECh. U1.4 - Prob. 6ECh. U1.4 - Prob. 7ECh. U1.4 - Prob. 8ECh. U1.4 - Prob. 9ECh. U1.4 - Prob. 10ECh. U1.4 - Prob. 11ECh. U1.5 - Prob. 1TAICh. U1.5 - Prob. 1ECh. U1.5 - Prob. 2ECh. U1.5 - Prob. 3ECh. U1.5 - Prob. 4ECh. U1.5 - Prob. 5ECh. U1.5 - Prob. 6ECh. U1.5 - Prob. 7ECh. U1.6 - Prob. 1TAICh. U1.6 - Prob. 1ECh. U1.6 - Prob. 2ECh. U1.6 - Prob. 3ECh. U1.6 - Prob. 4ECh. U1.6 - Prob. 5ECh. U1.6 - Prob. 6ECh. U1.7 - Prob. 1TAICh. U1.7 - Prob. 1ECh. U1.7 - Prob. 2ECh. U1.7 - Prob. 3ECh. U1.7 - Prob. 4ECh. U1.7 - Prob. 5ECh. U1.8 - Prob. 1TAICh. U1.8 - Prob. 1ECh. U1.8 - Prob. 2ECh. U1.8 - Prob. 4ECh. U1.8 - Prob. 5ECh. U1.8 - Prob. 6ECh. U1.8 - Prob. 7ECh. U1.9 - Prob. 1TAICh. U1.9 - Prob. 1ECh. U1.9 - Prob. 2ECh. U1.9 - Prob. 5ECh. U1.9 - Prob. 7ECh. U1.10 - Prob. 1TAICh. U1.10 - Prob. 1ECh. U1.10 - Prob. 2ECh. U1.10 - Prob. 3ECh. U1.10 - Prob. 4ECh. U1.10 - Prob. 5ECh. U1.10 - Prob. 6ECh. U1.10 - Prob. 7ECh. U1.10 - Prob. 8ECh. U1.11 - Prob. 1TAICh. U1.11 - Prob. 1ECh. U1.11 - Prob. 2ECh. U1.11 - Prob. 3ECh. U1.11 - Prob. 4ECh. U1.11 - Prob. 5ECh. U1.11 - Prob. 6ECh. U1.11 - Prob. 7ECh. U1.11 - Prob. 9ECh. U1.11 - Prob. 11ECh. U1.11 - Prob. 12ECh. U1.12 - Prob. 1TAICh. U1.12 - Prob. 1ECh. U1.12 - Prob. 2ECh. U1.12 - Prob. 3ECh. U1.12 - Prob. 4ECh. U1.12 - Prob. 5ECh. U1.12 - Prob. 6ECh. U1.12 - Prob. 7ECh. U1.12 - Prob. 8ECh. U1.13 - Prob. 1TAICh. U1.13 - Prob. 1ECh. U1.13 - Prob. 2ECh. U1.13 - Prob. 3ECh. U1.13 - Prob. 4ECh. U1.13 - Prob. 5ECh. U1.13 - Prob. 6ECh. U1.13 - Prob. 7ECh. U1.13 - Prob. 8ECh. U1.13 - Prob. 9ECh. U1.14 - Prob. 1TAICh. U1.14 - Prob. 1ECh. U1.14 - Prob. 2ECh. U1.14 - Prob. 3ECh. U1.14 - Prob. 4ECh. U1.14 - Prob. 5ECh. U1.14 - Prob. 6ECh. U1.14 - Prob. 7ECh. U1.14 - Prob. 8ECh. U1.14 - Prob. 9ECh. U1.14 - Prob. 10ECh. U1.14 - Prob. 11ECh. U1.14 - Prob. 12ECh. U1.14 - Prob. 13ECh. U1.14 - Prob. 14ECh. U1.15 - Prob. 1TAICh. U1.15 - Prob. 1ECh. U1.15 - Prob. 2ECh. U1.15 - Prob. 3ECh. U1.15 - Prob. 4ECh. U1.15 - Prob. 5ECh. U1.15 - Prob. 6ECh. U1.15 - Prob. 7ECh. U1.15 - Prob. 8ECh. U1.15 - Prob. 9ECh. U1.15 - Prob. 10ECh. U1.15 - Prob. 11ECh. U1.15 - Prob. 12ECh. U1.16 - Prob. 1TAICh. U1.16 - Prob. 1ECh. U1.16 - Prob. 2ECh. U1.16 - Prob. 3ECh. U1.16 - Prob. 4ECh. U1.16 - Prob. 5ECh. U1.16 - Prob. 6ECh. U1.17 - Prob. 1TAICh. U1.17 - Prob. 1ECh. U1.17 - Prob. 2ECh. U1.17 - Prob. 3ECh. U1.17 - Prob. 4ECh. U1.17 - Prob. 5ECh. U1.17 - Prob. 6ECh. U1.17 - Prob. 7ECh. U1.17 - Prob. 8ECh. U1.17 - Prob. 9ECh. U1.17 - Prob. 10ECh. U1.17 - Prob. 11ECh. U1.18 - Prob. 1TAICh. U1.18 - Prob. 1ECh. U1.18 - Prob. 2ECh. U1.18 - Prob. 3ECh. U1.18 - Prob. 4ECh. U1.18 - Prob. 5ECh. U1.18 - Prob. 6ECh. U1.18 - Prob. 7ECh. U1.18 - Prob. 8ECh. U1.18 - Prob. 9ECh. U1.18 - Prob. 10ECh. U1.19 - Prob. 1TAICh. U1.19 - Prob. 1ECh. U1.19 - Prob. 2ECh. U1.19 - Prob. 3ECh. U1.19 - Prob. 4ECh. U1.19 - Prob. 5ECh. U1.19 - Prob. 6ECh. U1.19 - Prob. 7ECh. U1.19 - Prob. 8ECh. U1.19 - Prob. 9ECh. U1.19 - Prob. 10ECh. U1.19 - Prob. 11ECh. U1.19 - Prob. 12ECh. U1.19 - Prob. 13ECh. U1.19 - Prob. 14ECh. U1.19 - Prob. 15ECh. U1.19 - Prob. 16ECh. U1.20 - Prob. 1TAICh. U1.20 - Prob. 1ECh. U1.20 - Prob. 2ECh. U1.20 - Prob. 3ECh. U1.20 - Prob. 4ECh. U1.20 - Prob. 5ECh. U1.20 - Prob. 6ECh. U1.20 - Prob. 7ECh. U1.21 - Prob. 1TAICh. U1.21 - Prob. 1ECh. U1.21 - Prob. 2ECh. U1.21 - Prob. 3ECh. U1.21 - Prob. 4ECh. U1.21 - Prob. 5ECh. U1.21 - Prob. 6ECh. U1.21 - Prob. 7ECh. U1.21 - Prob. 8ECh. U1.22 - Prob. 1TAICh. U1.22 - Prob. 1ECh. U1.22 - Prob. 2ECh. U1.22 - Prob. 3ECh. U1.22 - Prob. 4ECh. U1.22 - Prob. 5ECh. U1.22 - Prob. 6ECh. U1.22 - Prob. 7ECh. U1.23 - Prob. 1TAICh. U1.23 - Prob. 1ECh. U1.23 - Prob. 2ECh. U1.23 - Prob. 3ECh. U1.23 - Prob. 4ECh. U1.23 - Prob. 5ECh. U1.24 - Prob. 1TAICh. U1.24 - Prob. 1ECh. U1.24 - Prob. 2ECh. U1.24 - Prob. 3ECh. U1.24 - Prob. 4ECh. U1.24 - Prob. 5ECh. U1.24 - Prob. 6ECh. U1.24 - Prob. 7ECh. U1.24 - Prob. 8ECh. U1.24 - Prob. 9ECh. U1.24 - Prob. 10ECh. U1.24 - Prob. 11ECh. U1.24 - Prob. 12ECh. U1.24 - Prob. 13ECh. U1.25 - Prob. 1TAICh. U1.25 - Prob. 1ECh. U1.25 - Prob. 2ECh. U1.25 - Prob. 3ECh. U1.25 - Prob. 4ECh. U1.25 - Prob. 5ECh. U1.25 - Prob. 6ECh. U1.26 - Prob. 1TAICh. U1.26 - Prob. 1ECh. U1.26 - Prob. 2ECh. U1.26 - Prob. 3ECh. U1.26 - Prob. 4ECh. U1.26 - Prob. 5ECh. U1.26 - Prob. 6ECh. U1.26 - Prob. 7ECh. U1.26 - Prob. 8ECh. U1.26 - Prob. 9ECh. U1.26 - Prob. 10ECh. U1.27 - Prob. 1TAICh. U1.27 - Prob. 1ECh. U1.27 - Prob. 2ECh. U1.27 - Prob. 3ECh. U1.27 - Prob. 4ECh. U1.27 - Prob. 5ECh. U1.27 - Prob. 6ECh. U1.27 - Prob. 7ECh. U1 - Prob. C1.1RECh. U1 - Prob. C1.2RECh. U1 - Prob. C1.3RECh. U1 - Prob. C1.4RECh. U1 - Prob. C1.5RECh. U1 - Prob. C1.6RECh. U1 - Prob. C2.1RECh. U1 - Prob. C2.2RECh. U1 - Prob. C2.3RECh. U1 - Prob. C2.4RECh. U1 - Prob. C3.1RECh. U1 - Prob. C3.2RECh. U1 - Prob. C3.3RECh. U1 - Prob. C3.4RECh. U1 - Prob. C4.1RECh. U1 - Prob. C4.2RECh. U1 - Prob. C4.3RECh. U1 - Prob. C4.4RECh. U1 - Prob. C5.1RECh. U1 - Prob. C5.2RECh. U1 - Prob. C5.3RECh. U1 - Prob. C5.4RECh. U1 - Prob. 1RECh. U1 - Prob. 2RECh. U1 - Prob. 3RECh. U1 - Prob. 4RECh. U1 - Prob. 5RECh. U1 - Prob. 6RECh. U1 - Prob. 7RECh. U1 - Prob. 8RECh. U1 - Prob. 9RECh. U1 - Prob. 10RECh. U1 - Prob. 11RECh. U1 - Prob. 12RECh. U1 - Prob. 1STPCh. U1 - Prob. 2STPCh. U1 - Prob. 3STPCh. U1 - Prob. 4STPCh. U1 - Prob. 5STPCh. U1 - Prob. 6STPCh. U1 - Prob. 7STPCh. U1 - Prob. 8STPCh. U1 - Prob. 9STPCh. U1 - Prob. 10STPCh. U1 - Prob. 11STPCh. U1 - Prob. 12STPCh. U1 - Prob. 13STPCh. U1 - Prob. 14STPCh. U1 - Prob. 15STPCh. U1 - Prob. 16STPCh. U1 - Prob. 17STPCh. U1 - Prob. 18STPCh. U1 - Prob. 19STPCh. U1 - Prob. 20STPCh. U1 - Prob. 21STPCh. U1 - Prob. 22STP
Additional Science Textbook Solutions
Find more solutions based on key concepts
1. Compare and contrast the following terms:
a. dominant and recessive
b. genotype and phenotype
c. homozyg...
Genetic Analysis: An Integrated Approach (3rd Edition)
Why are BSL-4 suits pressurized? Why not just wear tough regular suits?
Microbiology with Diseases by Body System (5th Edition)
APPLY 1.2 Express the following quantities in scientific notation
using fundamental SI units of mass and lengt...
Chemistry (7th Edition)
Based on your answers to Questions 2 and 3, which part of the Atlantic basin appears to have opened first?
Applications and Investigations in Earth Science (9th Edition)
Which of the following factors would tend to increase membrane fluidity? A. a greater proportion of unsaturated...
Campbell Biology in Focus (2nd Edition)
47. A block hangs in equilibrium from a vertical spring. When a second identical block is added, the original ...
Physics for Scientists and Engineers: A Strategic Approach, Vol. 1 (Chs 1-21) (4th Edition)
Knowledge Booster
Similar questions
- You are trying to decide if there is a single reagent you can add that will make the following synthesis possible without any other major side products: xi 1. ☑ 2. H₂O хе i Draw the missing reagent X you think will make this synthesis work in the drawing area below. If there is no reagent that will make your desired product in good yield or without complications, just check the box under the drawing area and leave it blank. Click and drag to start drawing a structure. There is no reagent that will make this synthesis work without complications. : ☐ S ☐arrow_forwardPredict the major products of this organic reaction: H OH 1. LiAlH4 2. H₂O ? Note: be sure you use dash and wedge bonds when necessary, for example to distinguish between major products with different stereochemistry. Click and drag to start drawing a structure. G C टेarrow_forwardFor each reaction below, decide if the first stable organic product that forms in solution will create a new C-C bond, and check the appropriate box. Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below. Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first stable product you expect to form in solution. NH2 CI MgCl ? Will the first product that forms in this reaction create a new CC bond? Yes No MgBr ? Will the first product that forms in this reaction create a new CC bond? Yes No G टेarrow_forward
- For each reaction below, decide if the first stable organic product that forms in solution will create a new CC bond, and check the appropriate box. Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below. Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first stable product you expect to form in solution. དྲ。 ✗MgBr ? O CI Will the first product that forms in this reaction create a new C-C bond? Yes No • ? Will the first product that forms in this reaction create a new CC bond? Yes No × : ☐ Xarrow_forwardPredict the major products of this organic reaction: OH NaBH4 H ? CH3OH Note: be sure you use dash and wedge bonds when necessary, for example to distinguish between major products with different stereochemistry. Click and drag to start drawing a structure. ☐ : Sarrow_forwardPredict the major products of this organic reaction: 1. LIAIHA 2. H₂O ? Note: be sure you use dash and wedge bonds when necessary, for example to distinguish between major products with different stereochemistry. Click and drag to start drawing a structure. X : ☐arrow_forward
- For each reaction below, decide if the first stable organic product that forms in solution will create a new C - C bond, and check the appropriate box. Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below. Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first stable product you expect to form in solution. NH2 tu ? ? OH Will the first product that forms in this reaction create a new CC bond? Yes No Will the first product that forms in this reaction create a new CC bond? Yes No C $ ©arrow_forwardAs the lead product manager at OrganometALEKS Industries, you are trying to decide if the following reaction will make a molecule with a new C-C bond as its major product: 1. MgCl ? 2. H₂O* If this reaction will work, draw the major organic product or products you would expect in the drawing area below. If there's more than one major product, you can draw them in any arrangement you like. Be sure you use wedge and dash bonds if necessary, for example to distinguish between major products with different stereochemistry. If the major products of this reaction won't have a new CC bond, just check the box under the drawing area and leave it blank. Click and drag to start drawing a structure. This reaction will not make a product with a new CC bond. G marrow_forwardIncluding activity coefficients, find [Hg22+] in saturated Hg2Br2 in 0.00100 M NH4 Ksp Hg2Br2 = 5.6×10-23.arrow_forward
- give example for the following(by equation) a. Converting a water insoluble compound to a soluble one. b. Diazotization reaction form diazonium salt c. coupling reaction of a diazonium salt d. indacator properties of MO e. Diazotization ( diazonium salt of bromobenzene)arrow_forward2-Propanone and ethyllithium are mixed and subsequently acid hydrolyzed. Draw and name the structures of the products.arrow_forward(Methanesulfinyl)methane is reacted with NaH, and then with acetophenone. Draw and name the structures of the products.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
ChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill Education
Principles of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill Education
Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
Elementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY