Interpretation:
The contaminants that pose immediate health risks and the contaminants that can be eliminated by boiling are to be stated.
Concept Introduction:
Water is a common liquid that is present on the Earth.
It is also known as universal solvent. It can dissolve a wide range of organic and inorganic solutes.
Water is vital for the existence of all living animals. Without water, no life form can exist, it constitutes an important part of rivers, lakes, streams, clouds, snow and ice.
Water is truly an unusual molecule such that being a low molar mass compound, it exists as a liquid at room temperature and has an anonymously high boiling point.
Ice floats on water because it has a lower density than water.
Water contains some unwanted particles which can lead to diseases and other hostile effects on human health.
Numerous types of micro-organisms such as bacteria are present in water, which contaminate the water.
Biological contaminants: Some microbes can live in water and can cause various diseases like cholera, dysentery, and so on. Two examples of such microbes are Giardia and Legionella.
Inorganic contaminants: Some inorganic molecules can dissolve in water and make it impotable (not suited for drinking). Two examples of such molecules are Nitrates and Asbestos.
Organic contaminants: Some organic molecules can dissolve in water and makes it impotable (not suited for drinking). Two examples of such molecules are chlorohydrocarbons (volatile) and ethylbenzene (non-volatile).
Radioactive contaminants: Some radioactive elements can dissolve in water and make it impotable (not suited for drinking). Two examples of such elements are Uranium and Radium.
Contaminants that pose immediate health risks are the biological contaminants and inorganic contaminants because they get immediately dissolved in blood and starts reacting with it.
Contaminants that can be eliminated by boiling are the biological contaminants because the microbes can be killed by increasing the temperature.

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Chapter 12 Solutions
Bundle: Chemistry In Focus: A Molecular View Of Our World, 7th + Owlv2 With Mindtap Reader, 1 Term (6 Months) Printed Access Card
- Explanation Check Draw the skeletal ("line") structure of 5-hydroxy-4-methyl-2-pentanone. Click and drag to start drawing a structure. Х © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Cer ☐ : Carrow_forward1. Using a Model set Build a model for the following compound [CH2BrCI]. 2. Build another model of the mirror image of your first molecule. 3. Place the two models next to each other and take a picture which shows the differences between the two models. 4. Determine the absolute stereochemistry R or S for the two models. 5. Write or type a paragraph to Discuss the stereochemical relationship between the two models of CH2BrCl. You must provide an explanation for your conclusions also provide a description for the colors used to represent each atom in the model's images.arrow_forwardWhat parameters are included in the specific rotation calculation of a pure substance based on measurement from a polarimeter? Select one or more: Density of the sample Pathlength of the sample container Enantiomeric excess of the sample Measured rotation of lightarrow_forward
- V Determine whether the following molecule is a hemiacetal, acetal, or neither and select the appropriate box below. Also, highlight the hemiacetal or acetal carbon if there is one. Explanation O CH O Ohemiacetal Oacetal Oneither Check A 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use Privacy Cer 000 Ararrow_forward1. Using Online resources and chemical structures hand draw four different organic compounds (not those already shown in your handout) that are chiral, optically active (a pair of enantiomers will count as one). Pay attention to correct stereochemistry 2. Write or type a short paragraph to Discuss the stereochemical relationship between the four compounds.arrow_forward1. Using a Model set Build a model for the following compound [CHBRIF] 2. Build another model of the mirror image of your first molecule. 3. Place the two models next to each other and take a picture which shows the differences between the two models. 4. Determine the absolute stereochemistry R or S for the two models. 5. Write or type a paragraph to Discuss the stereochemical relationship between the two models of CHBгCIF. You must provide an explanation for your conclusions also provide a description for the colors used to representarrow_forward
- The specific rotation of a sample depends upon measured angle of rotation, the density of the sample, and the pathway length of the light. True Falsearrow_forwardConsider the molecule A,B, C and D shown below, (1 x 4) Br NH2 A OH Br 边 H B C D 1. Assign the R/S configuration to each chiral center and identify by circling all the chiral centers. 2. Draw an image for the enantiomer of each of the compounds A, B, C and D.arrow_forwardCould you crystallize one enantiomer of mandelic acid from a racemic mixture (using the typical achiral solvents found in our lab) without preparing a diastereomeric salt? Why or why not? No, because both enantiomers have the same solubility in achiral solvents. than the other. ооо Yes, because one enantiomer has a higher melting point No, because both enantiomers are liquids. Yes, because one enantiomer is more crystalline than the other.arrow_forward
- If the literature value of specific rotation for a chiral compound is -53.6°, what is the enantiomeric excess of a compound with a measured specific rotation of -40.5°?arrow_forwardThe process to determine the configuration, starts by placing the lowest priority substituent toward the back. If the substituents pointing forward decrease in priority in a clockwise order, the configuration is S. If the substituents decrease in priority in a counterclockwise order, the configuration is R. True Falsearrow_forwardIn the drawing area below, create a hemiacetal with 1 hydroxyl group, 1 methoxy group, and a total of 3 carbon atoms. Click and drag to start drawing a structure. Explanation Check Х PO 18 Ar B © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibilityarrow_forward
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