Living By Chemistry: First Edition Textbook
1st Edition
ISBN: 9781559539418
Author: Angelica Stacy
Publisher: MAC HIGHER
expand_more
expand_more
format_list_bulleted
Question
Chapter U5.5, Problem 10E
Interpretation Introduction
Interpretation:
Farmers spray water on oranges to protect them from frost, reason behind this needs to be explained.
Concept Introduction :
The latent heat of vaporization is also recognized as the enthalpy of evaporation or vaporization. It is the amount of energy which must be added to a liquid substance, to alter a given amount of the substance into a gas.
Expert Solution & Answer
Answer to Problem 10E
To preserve oranges from freezing.
Explanation of Solution
When an orange farm is forecasted for freezing, the farmers usually sprays water to the trees. When there is a drop in temperature, this water freezes and heat is released into the environment.
This is quite enough heat to keep the fruit preserved from freezing. Thus, causing an ice to form on the oranges actually saves them from freezing.
Chapter U5 Solutions
Living By Chemistry: First Edition Textbook
Ch. U5.1 - Prob. 1TAICh. U5.1 - Prob. 1ECh. U5.1 - Prob. 2ECh. U5.1 - Prob. 3ECh. U5.1 - Prob. 4ECh. U5.1 - Prob. 5ECh. U5.1 - Prob. 6ECh. U5.2 - Prob. 1TAICh. U5.2 - Prob. 1ECh. U5.2 - Prob. 2E
Ch. U5.2 - Prob. 3ECh. U5.2 - Prob. 4ECh. U5.2 - Prob. 5ECh. U5.3 - Prob. 1TAICh. U5.3 - Prob. 1ECh. U5.3 - Prob. 2ECh. U5.3 - Prob. 3ECh. U5.3 - Prob. 4ECh. U5.3 - Prob. 5ECh. U5.3 - Prob. 6ECh. U5.3 - Prob. 7ECh. U5.3 - Prob. 8ECh. U5.3 - Prob. 9ECh. U5.3 - Prob. 10ECh. U5.3 - Prob. 11ECh. U5.4 - Prob. 1TAICh. U5.4 - Prob. 1ECh. U5.4 - Prob. 2ECh. U5.4 - Prob. 3ECh. U5.4 - Prob. 4ECh. U5.4 - Prob. 5ECh. U5.4 - Prob. 6ECh. U5.4 - Prob. 7ECh. U5.5 - Prob. 1TAICh. U5.5 - Prob. 1ECh. U5.5 - Prob. 2ECh. U5.5 - Prob. 3ECh. U5.5 - Prob. 4ECh. U5.5 - Prob. 5ECh. U5.5 - Prob. 6ECh. U5.5 - Prob. 7ECh. U5.5 - Prob. 8ECh. U5.5 - Prob. 9ECh. U5.5 - Prob. 10ECh. U5.6 - Prob. 1TAICh. U5.6 - Prob. 1ECh. U5.6 - Prob. 2ECh. U5.6 - Prob. 3ECh. U5.6 - Prob. 4ECh. U5.6 - Prob. 5ECh. U5.6 - Prob. 6ECh. U5.6 - Prob. 7ECh. U5.6 - Prob. 8ECh. U5.6 - Prob. 9ECh. U5.7 - Prob. 1TAICh. U5.7 - Prob. 1ECh. U5.7 - Prob. 2ECh. U5.7 - Prob. 3ECh. U5.7 - Prob. 4ECh. U5.7 - Prob. 5ECh. U5.8 - Prob. 1TAICh. U5.8 - Prob. 1ECh. U5.8 - Prob. 2ECh. U5.8 - Prob. 3ECh. U5.8 - Prob. 4ECh. U5.8 - Prob. 6ECh. U5.9 - Prob. 1TAICh. U5.9 - Prob. 1ECh. U5.9 - Prob. 2ECh. U5.9 - Prob. 3ECh. U5.9 - Prob. 4ECh. U5.9 - Prob. 5ECh. U5.9 - Prob. 6ECh. U5.9 - Prob. 8ECh. U5.10 - Prob. 1TAICh. U5.10 - Prob. 1ECh. U5.10 - Prob. 2ECh. U5.10 - Prob. 3ECh. U5.10 - Prob. 4ECh. U5.10 - Prob. 5ECh. U5.10 - Prob. 6ECh. U5.11 - Prob. 1TAICh. U5.11 - Prob. 1ECh. U5.11 - Prob. 2ECh. U5.11 - Prob. 3ECh. U5.11 - Prob. 4ECh. U5.11 - Prob. 5ECh. U5.11 - Prob. 6ECh. U5.11 - Prob. 7ECh. U5.11 - Prob. 8ECh. U5.11 - Prob. 9ECh. U5.12 - Prob. 1TAICh. U5.12 - Prob. 1ECh. U5.12 - Prob. 2ECh. U5.12 - Prob. 3ECh. U5.12 - Prob. 4ECh. U5.12 - Prob. 5ECh. U5.13 - Prob. 1TAICh. U5.13 - Prob. 1ECh. U5.13 - Prob. 2ECh. U5.13 - Prob. 3ECh. U5.13 - Prob. 4ECh. U5.13 - Prob. 5ECh. U5.13 - Prob. 6ECh. U5.13 - Prob. 7ECh. U5.13 - Prob. 8ECh. U5.13 - Prob. 9ECh. U5.13 - Prob. 11ECh. U5.14 - Prob. 1TAICh. U5.14 - Prob. 1ECh. U5.14 - Prob. 2ECh. U5.14 - Prob. 3ECh. U5.14 - Prob. 4ECh. U5.15 - Prob. 1TAICh. U5.15 - Prob. 1ECh. U5.15 - Prob. 2ECh. U5.15 - Prob. 3ECh. U5.15 - Prob. 4ECh. U5.15 - Prob. 5ECh. U5.16 - Prob. 1TAICh. U5.16 - Prob. 1ECh. U5.16 - Prob. 2ECh. U5.16 - Prob. 3ECh. U5.16 - Prob. 4ECh. U5.16 - Prob. 5ECh. U5.16 - Prob. 6ECh. U5.16 - Prob. 7ECh. U5.16 - Prob. 8ECh. U5.17 - Prob. 1TAICh. U5.17 - Prob. 1ECh. U5.17 - Prob. 2ECh. U5.17 - Prob. 3ECh. U5.17 - Prob. 4ECh. U5.17 - Prob. 5ECh. U5.17 - Prob. 6ECh. U5.17 - Prob. 7ECh. U5.18 - Prob. 1TAICh. U5.18 - Prob. 1ECh. U5.18 - Prob. 2ECh. U5.18 - Prob. 3ECh. U5.18 - Prob. 4ECh. U5.18 - Prob. 5ECh. U5.18 - Prob. 6ECh. U5.18 - Prob. 7ECh. U5.18 - Prob. 8ECh. U5.18 - Prob. 9ECh. U5.19 - Prob. 1TAICh. U5.19 - Prob. 1ECh. U5.19 - Prob. 2ECh. U5.19 - Prob. 3ECh. U5.19 - Prob. 4ECh. U5.19 - Prob. 5ECh. U5.19 - Prob. 6ECh. U5.19 - Prob. 7ECh. U5 - Prob. SI1RECh. U5 - Prob. SI2RECh. U5 - Prob. SI3RECh. U5 - Prob. SI4RECh. U5 - Prob. SI5RECh. U5 - Prob. SI6RECh. U5 - Prob. SI7RECh. U5 - Prob. SI8RECh. U5 - Prob. SII1RECh. U5 - Prob. SII2RECh. U5 - Prob. SII3RECh. U5 - Prob. SII4RECh. U5 - Prob. SIII1RECh. U5 - Prob. SIII2RECh. U5 - Prob. SIII3RECh. U5 - Prob. SIII4RECh. U5 - Prob. SIII6RECh. U5 - Prob. SIV1RECh. U5 - Prob. SIV2RECh. U5 - Prob. SIV3RECh. U5 - Prob. SIV4RECh. U5 - Prob. SIV5RECh. U5 - Prob. 1RECh. U5 - Prob. 2RECh. U5 - Prob. 3RECh. U5 - Prob. 4RECh. U5 - Prob. 5RECh. U5 - Prob. 6RECh. U5 - Prob. 7RECh. U5 - Prob. 8RECh. U5 - Prob. 9RECh. U5 - Prob. 10RECh. U5 - Prob. 11RECh. U5 - Prob. 12RECh. U5 - Prob. 13RECh. U5 - Prob. 14RECh. U5 - Prob. 15RE
Additional Science Textbook Solutions
Find more solutions based on key concepts
36. If a cell’s membrane thickness doubles but the cell stays the same size, how do the resistance and the capa...
College Physics: A Strategic Approach (3rd Edition)
Match each of the following items with all the terms it applies to:
Human Physiology: An Integrated Approach (8th Edition)
If an egg rolls out of the nest, a mother greylag goose will retrieve it by nudging it with her beak and head. ...
Campbell Biology (11th Edition)
Using the South Atlantic as an example, label the beginning of the normal polarity period C that began 2 millio...
Applications and Investigations in Earth Science (9th Edition)
Explain all answers clearly, with complete sentences and proper essay structure if needed. An asterisk (*) desi...
Cosmic Perspective Fundamentals
The bond angles in a regular polygon with n sides are equal to 180360n a. What are the bond angles in a regular...
Organic Chemistry (8th Edition)
Knowledge Booster
Similar questions
- 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. ? NH2 MgBr 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? O Yes O No Click and drag to start drawing a structure. :☐ G x c olo Ar HEarrow_forwardPredicting 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: H₂N O H 1. ? 2. H3O+ 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. 0 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. فا Explanation Check Click and drag to start drawing a structure.arrow_forwardHighlight the chirality (or stereogenic) center(s) in the given compound. A compound may have one or more stereogenic centers. OH OH OH OH OH OHarrow_forward
- Using wedge-and-dash bonds, modify the bonds on the chiral carbon in the molecule below so the molecule has R stereochemical configuration. NH H Br X टेarrow_forwardProvide photos of models of the following molecules. (Include a key for identification of the atoms) 1,2-dichloropropane 2,3,3-trimethylhexane 2-bromo-3-methybutanearrow_forwardPlease draw the structure in the box that is consistent with all the spectral data and alphabetically label all of the equivalent protons in the structure (Ha, Hb, Hc....) in order to assign all the proton NMR peaks. The integrations are computer generated and approximate the number of equivalent protons. Molecular formula: C13H1802 14 13 12 11 10 11 (ppm) Structure with assigned H peaks 2.08 3.13arrow_forward
- A 0.10 M solution of acetic acid (CH3COOH, Ka = 1.8 x 10^-5) is titrated with a 0.0250 M solution of magnesium hydroxide (Mg(OH)2). If 10.0 mL of the acid solution is titrated with 10.0 mL of the base solution, what is the pH of the resulting solution?arrow_forwardFirefly luciferin exhibits three rings. Identify which of the rings are aromatic. Identify which lone pairs are involved in establishing aromaticity. The lone pairs are labeled A-D below.arrow_forwardA 0.10 M solution of acetic acid (CH3COOH, Ka = 1.8 x 10^-5) is titrated with a 0.0250 M solution of magnesium hydroxide (Mg(OH)2). If 10.0 mL of the acid solution is titrated with 10.0 mL of the base solution, what is the pH of the resulting solution?arrow_forward
- Given a complex reaction with rate equation v = k1[A] + k2[A]2, what is the overall reaction order?arrow_forwardPlease draw the structure in the box that is consistent with all the spectral data and alphabetically label all of the equivalent protons in the structure (Ha, Hb, Hc....) in order to assign all the proton NMR peaks. The integrations are computer generated and approximate the number of equivalent protons. Molecular formula: C13H1802 14 13 12 11 10 11 (ppm) Structure with assigned H peaks 2.08 3.13arrow_forwardCHEMICAL KINETICS. One of the approximation methods for solving the rate equation is the steady-state approximation method. Explain what it consists of.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