Living by Chemistry
2nd Edition
ISBN: 9781464142314
Author: Angelica M. Stacy
Publisher: W. H. Freeman
expand_more
expand_more
format_list_bulleted
Question
Chapter U4.68, Problem 6E
Interpretation Introduction
Interpretation:
At least three types of effects that a toxic substance can have on the body must be described.
Concept introduction:
Toxic substances are those which have bad influence on living beings. It can be a gas which creates problem when inhaled. It can be a solid or liquid which have serious effects when it enters inside the body.
Expert Solution & Answer
Answer to Problem 6E
Three types of effects that a toxic substance can have on the body are as follows:
Difficulty in breathing, vomiting and headache.
Explanation of Solution
Different toxic substances have different effects on the body. Some of the substance create breathing problems. For example, phosphine (PH3) gas. Some of the toxic substances when consumed with food or through other sources can cause vomiting. For example, diphenylchloroarsine and diphenylcyanoarsine.Some toxic substances such as carbon monoxide, benzol, and nitroglycerine are responsible for headache.
Chapter U4 Solutions
Living by Chemistry
Ch. U4.68 - Prob. 1TAICh. U4.68 - Prob. 1ECh. U4.68 - Prob. 2ECh. U4.68 - Prob. 3ECh. U4.68 - Prob. 4ECh. U4.68 - Prob. 5ECh. U4.68 - Prob. 6ECh. U4.69 - Prob. 1TAICh. U4.69 - Prob. 1ECh. U4.69 - Prob. 2E
Ch. U4.69 - Prob. 3ECh. U4.69 - Prob. 4ECh. U4.69 - Prob. 5ECh. U4.70 - Prob. 1TAICh. U4.70 - Prob. 1ECh. U4.70 - Prob. 2ECh. U4.70 - Prob. 3ECh. U4.70 - Prob. 4ECh. U4.70 - Prob. 6ECh. U4.71 - Prob. 1TAICh. U4.71 - Prob. 1ECh. U4.71 - Prob. 2ECh. U4.71 - Prob. 3ECh. U4.71 - Prob. 4ECh. U4.71 - Prob. 5ECh. U4.71 - Prob. 6ECh. U4.71 - Prob. 7ECh. U4.72 - Prob. 1TAICh. U4.72 - Prob. 1ECh. U4.72 - Prob. 2ECh. U4.72 - Prob. 3ECh. U4.72 - Prob. 4ECh. U4.73 - Prob. 1TAICh. U4.73 - Prob. 1ECh. U4.73 - Prob. 2ECh. U4.73 - Prob. 3ECh. U4.73 - Prob. 5ECh. U4.73 - Prob. 6ECh. U4.73 - Prob. 7ECh. U4.74 - Prob. 1TAICh. U4.74 - Prob. 1ECh. U4.74 - Prob. 2ECh. U4.74 - Prob. 4ECh. U4.74 - Prob. 5ECh. U4.75 - Prob. 1TAICh. U4.75 - Prob. 1ECh. U4.75 - Prob. 2ECh. U4.75 - Prob. 4ECh. U4.75 - Prob. 5ECh. U4.75 - Prob. 6ECh. U4.75 - Prob. 7ECh. U4.75 - Prob. 8ECh. U4.75 - Prob. 9ECh. U4.75 - Prob. 10ECh. U4.75 - Prob. 11ECh. U4.76 - Prob. 1TAICh. U4.76 - Prob. 1ECh. U4.76 - Prob. 2ECh. U4.76 - Prob. 3ECh. U4.76 - Prob. 4ECh. U4.76 - Prob. 5ECh. U4.76 - Prob. 6ECh. U4.76 - Prob. 7ECh. U4.76 - Prob. 8ECh. U4.77 - Prob. 1TAICh. U4.77 - Prob. 1ECh. U4.77 - Prob. 2ECh. U4.77 - Prob. 3ECh. U4.77 - Prob. 4ECh. U4.77 - Prob. 5ECh. U4.77 - Prob. 6ECh. U4.77 - Prob. 7ECh. U4.77 - Prob. 8ECh. U4.78 - Prob. 1TAICh. U4.78 - Prob. 1ECh. U4.78 - Prob. 2ECh. U4.78 - Prob. 3ECh. U4.78 - Prob. 4ECh. U4.78 - Prob. 5ECh. U4.78 - Prob. 6ECh. U4.78 - Prob. 7ECh. U4.78 - Prob. 8ECh. U4.79 - Prob. 1TAICh. U4.79 - Prob. 1ECh. U4.79 - Prob. 2ECh. U4.79 - Prob. 3ECh. U4.79 - Prob. 4ECh. U4.80 - Prob. 1TAICh. U4.80 - Prob. 1ECh. U4.80 - Prob. 2ECh. U4.80 - Prob. 3ECh. U4.80 - Prob. 4ECh. U4.80 - Prob. 5ECh. U4.80 - Prob. 6ECh. U4.80 - Prob. 7ECh. U4.80 - Prob. 8ECh. U4.80 - Prob. 9ECh. U4.80 - Prob. 10ECh. U4.81 - Prob. 1TAICh. U4.81 - Prob. 1ECh. U4.81 - Prob. 2ECh. U4.81 - Prob. 3ECh. U4.81 - Prob. 4ECh. U4.81 - Prob. 5ECh. U4.81 - Prob. 6ECh. U4.81 - Prob. 7ECh. U4.81 - Prob. 8ECh. U4.81 - Prob. 9ECh. U4.82 - Prob. 1TAICh. U4.82 - Prob. 1ECh. U4.82 - Prob. 2ECh. U4.82 - Prob. 3ECh. U4.82 - Prob. 4ECh. U4.82 - Prob. 5ECh. U4.82 - Prob. 6ECh. U4.82 - Prob. 7ECh. U4.82 - Prob. 8ECh. U4.83 - Prob. 1TAICh. U4.83 - Prob. 1ECh. U4.83 - Prob. 2ECh. U4.83 - Prob. 3ECh. U4.83 - Prob. 4ECh. U4.83 - Prob. 5ECh. U4.83 - Prob. 6ECh. U4.83 - Prob. 7ECh. U4.84 - Prob. 1TAICh. U4.84 - Prob. 1ECh. U4.84 - Prob. 2ECh. U4.84 - Prob. 3ECh. U4.84 - Prob. 5ECh. U4.84 - Prob. 6ECh. U4.84 - Prob. 7ECh. U4.85 - Prob. 1TAICh. U4.85 - Prob. 1ECh. U4.85 - Prob. 2ECh. U4.85 - Prob. 3ECh. U4.85 - Prob. 4ECh. U4.85 - Prob. 5ECh. U4.85 - Prob. 6ECh. U4.85 - Prob. 7ECh. U4.85 - Prob. 8ECh. U4.86 - Prob. 1TAICh. U4.86 - Prob. 1ECh. U4.86 - Prob. 2ECh. U4.86 - Prob. 3ECh. U4.86 - Prob. 4ECh. U4.86 - Prob. 6ECh. U4.86 - Prob. 7ECh. U4.86 - Prob. 8ECh. U4.87 - Prob. 1TAICh. U4.87 - Prob. 1ECh. U4.87 - Prob. 2ECh. U4.87 - Prob. 3ECh. U4.87 - Prob. 4ECh. U4.87 - Prob. 5ECh. U4.87 - Prob. 6ECh. U4.87 - Prob. 7ECh. U4.87 - Prob. 8ECh. U4.88 - Prob. 1TAICh. U4.88 - Prob. 1ECh. U4.88 - Prob. 2ECh. U4.88 - Prob. 4ECh. U4.88 - Prob. 5ECh. U4.88 - Prob. 6ECh. U4.88 - Prob. 7ECh. U4.88 - Prob. 8ECh. U4.89 - Prob. 1TAICh. U4.89 - Prob. 1ECh. U4.89 - Prob. 2ECh. U4.89 - Prob. 3ECh. U4.89 - Prob. 4ECh. U4.89 - Prob. 5ECh. U4.89 - Prob. 6ECh. U4.90 - Prob. 1ECh. U4.90 - Prob. 2ECh. U4.90 - Prob. 3ECh. U4.90 - Prob. 4ECh. U4.90 - Prob. 5ECh. U4.90 - Prob. 6ECh. U4.90 - Prob. 7ECh. U4.91 - Prob. 1ECh. U4.91 - Prob. 2ECh. U4.91 - Prob. 3ECh. U4.91 - Prob. 5ECh. U4.91 - Prob. 6ECh. U4.92 - Prob. 1TAICh. U4.92 - Prob. 1ECh. U4.92 - Prob. 2ECh. U4.92 - Prob. 3ECh. U4.92 - Prob. 4ECh. U4.93 - Prob. 1TAICh. U4.93 - Prob. 1ECh. U4.93 - Prob. 2ECh. U4.93 - Prob. 4ECh. U4.93 - Prob. 5ECh. U4.93 - Prob. 6ECh. U4 - Prob. C13.3RECh. U4 - Prob. C13.4RECh. U4 - Prob. C14.1RECh. U4 - Prob. C14.2RECh. U4 - Prob. C14.3RECh. U4 - Prob. C14.5RECh. U4 - Prob. C14.6RECh. U4 - Prob. C15.1RECh. U4 - Prob. C15.2RECh. U4 - Prob. C15.3RECh. U4 - Prob. C15.4RECh. U4 - Prob. C15.5RECh. U4 - Prob. C15.6RECh. U4 - Prob. C15.7RECh. U4 - Prob. C15.8RECh. U4 - Prob. C16.1RECh. U4 - Prob. C16.2RECh. U4 - Prob. C16.3RECh. U4 - Prob. C16.4RECh. U4 - Prob. C17.1RECh. U4 - Prob. C17.2RECh. U4 - Prob. C17.3RECh. U4 - Prob. 1RECh. U4 - Prob. 4RECh. U4 - Prob. 5RECh. U4 - Prob. 6RECh. U4 - Prob. 7RECh. U4 - Prob. 8RECh. U4 - Prob. 9RECh. U4 - Prob. 10RECh. U4 - Prob. 11RECh. U4 - Prob. 12RECh. U4 - Prob. 1STPCh. U4 - Prob. 2STPCh. U4 - Prob. 3STPCh. U4 - Prob. 4STPCh. U4 - Prob. 5STPCh. U4 - Prob. 6STPCh. U4 - Prob. 7STPCh. U4 - Prob. 8STPCh. U4 - Prob. 9STPCh. U4 - Prob. 10STPCh. U4 - Prob. 11STPCh. U4 - Prob. 12STPCh. U4 - Prob. 13STPCh. U4 - Prob. 14STPCh. U4 - Prob. 15STPCh. U4 - Prob. 16STPCh. U4 - Prob. 17STPCh. U4 - Prob. 18STPCh. U4 - Prob. 19STPCh. U4 - Prob. 20STP
Additional Science Textbook Solutions
Find more solutions based on key concepts
WHAT IF? Is allopatric speciation more likely to occur on an island close to a mainland or on a more isolated i...
Campbell Biology in Focus (2nd Edition)
What global policy changes and what individual choices can help us sustain the planet that sustains us?
Biology: Life on Earth with Physiology (11th Edition)
The following data were obtained from a disk-diffusion test. Antibiotic Zone of Inhibition A 15 mm B 0 mm c 7 m...
Microbiology: An Introduction
4. Three groups of nonvascular plants are _______, ______, and _______. Three groups of seedless vascular plant...
Biology: Life on Earth (11th Edition)
Distinguish between microevolution, speciation, and macroevolution.
Campbell Essential Biology (7th Edition)
If someone at the other end of a room smokes a cigarette, you may breathe in some smoke. The movement of smoke ...
Campbell Essential Biology with Physiology (5th Edition)
Knowledge Booster
Similar questions
- 20. The Brusselator. This hypothetical system was first proposed by a group work- ing in Brussels [see Prigogine and Lefever (1968)] in connection with spatially nonuniform chemical patterns. Because certain steps involve trimolecular reac tions, it is not a model of any real chemical system but rather a prototype that has been studied extensively. The reaction steps are A-X. B+X-Y+D. 2X+ Y-3X, X-E. 305 It is assumed that concentrations of A, B, D, and E are kept artificially con stant so that only X and Y vary with time. (a) Show that if all rate constants are chosen appropriately, the equations de scribing a Brusselator are: dt A-(B+ 1)x + x²y, dy =Bx-x²y. diarrow_forwardProblem 3. Provide a mechanism for the following transformation: H₂SO A Me. Me Me Me Mearrow_forwardYou 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_forward
- Predict 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_forwardFor 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_forward
- Predict 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_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 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_forward
- As 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_forwardgive 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_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