
Chemistry in Context
8th Edition
ISBN: 9780073522975
Author: American Chemical Society
Publisher: McGraw-Hill Education
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Question
Chapter 11, Problem 56Q
(a)
Interpretation Introduction
Interpretation:
The reason for developing soy-rather than wheat-based food products for distribution in parts of the world where protein deficiency is a problem has to be explained.
Concept introduction:
Macronutrients:
- • They are required in relatively large amounts.
- • Required for the growth,
metabolism and other body functions. - • Calories are included in the compounds containing macronutrients.
- • There will be no toxic effect in their higher concentration.
- • Examples include carbohydrates, proteins and fats.
(b)
Interpretation Introduction
Interpretation:
The cultural reasons for prefering soy than wheat in some areas of the world should be suggested.
Concept introduction:
Macronutrients:
- • They are required in relatively large amounts.
- • Required for the growth, metabolism and other body functions.
- • Calories are included in the compounds containing macronutrients.
- • There will be no toxic effect in their higher concentration.
- • Examples include carbohydrates, proteins and fats.
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Draw the stepwise mechanism for the reactions
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Chapter 11 Solutions
Chemistry in Context
Ch. 11.2 - You Decide A Lifetime of Food During your...Ch. 11.4 - Prob. 11.8CTCh. 11.4 - Prob. 11.10YTCh. 11.5 - Prob. 11.11YTCh. 11.6 - Prob. 11.12CTCh. 11.6 - Prob. 11.13CTCh. 11.7 - Prob. 11.14YTCh. 11.8 - Prob. 11.15CTCh. 11.8 - Prob. 11.16CTCh. 11.8 - Prob. 11.17CT
Ch. 11.8 - You Decide Sodium in Your Diet Compare the sodium...Ch. 11.8 - Prob. 11.19CTCh. 11.9 - Prob. 11.20SCCh. 11.9 - Prob. 11.21YTCh. 11.11 - Prob. 11.25YTCh. 11.12 - a. Ammonia (NH3) is applied to soil in the form of...Ch. 11.12 - Prob. 11.27YTCh. 11 - One theme in this chapter is that what you eat...Ch. 11 - Prob. 3QCh. 11 - Prob. 4QCh. 11 - Prob. 5QCh. 11 - Prob. 6QCh. 11 - Prob. 7QCh. 11 - Prob. 8QCh. 11 - Prob. 9QCh. 11 - Prob. 10QCh. 11 - Prob. 11QCh. 11 - Prob. 12QCh. 11 - Prob. 13QCh. 11 - Prob. 14QCh. 11 - Prob. 15QCh. 11 - Prob. 16QCh. 11 - Prob. 17QCh. 11 - Prob. 18QCh. 11 - Prob. 19QCh. 11 - Prob. 20QCh. 11 - Prob. 21QCh. 11 - Prob. 22QCh. 11 - Prob. 23QCh. 11 - Prob. 24QCh. 11 - Prob. 25QCh. 11 - Prob. 26QCh. 11 - Prob. 27QCh. 11 - Prob. 28QCh. 11 - Prob. 29QCh. 11 - Prob. 30QCh. 11 - Prob. 31QCh. 11 - Prob. 32QCh. 11 - Explain to a friend why it is impossible to go on...Ch. 11 - Prob. 34QCh. 11 - Prob. 35QCh. 11 - Prob. 36QCh. 11 - Prob. 37QCh. 11 - Prob. 38QCh. 11 - Prob. 39QCh. 11 - Here is the condensed structural formula for...Ch. 11 - Prob. 41QCh. 11 - Prob. 42QCh. 11 - Prob. 43QCh. 11 - Prob. 44QCh. 11 - Prob. 45QCh. 11 - Prob. 46QCh. 11 - Prob. 47QCh. 11 - Biodiesel is another example of a biofuel. Answer...Ch. 11 - Prob. 49QCh. 11 - This chapter (together with Section 5.15) provided...Ch. 11 - Prob. 52QCh. 11 - Prob. 53QCh. 11 - Consider this structural formula for one of the...Ch. 11 - Prob. 56QCh. 11 - Prob. 57QCh. 11 - Prob. 59QCh. 11 - Prob. 60Q
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- Part I. Draw reaction mechanism for the transformations of benzophenone to benzopinacol to benzopinaco lone and answer the ff: Pinacol (2,3-dimethyl, 1-3-butanediol) on treatment w/ acid gives a mixture of pina colone and (3,3-dimethyl-2-butanone) 2,3-dimethyl-1,3-butadiene. Give reasonable mechanism the formation of the products Forarrow_forwardShow the mechanism for these reactionsarrow_forwardDraw the stepwise mechanismarrow_forward
- Draw a structural formula of the principal product formed when benzonitrile is treated with each reagent. (a) H₂O (one equivalent), H₂SO₄, heat (b) H₂O (excess), H₂SO₄, heat (c) NaOH, H₂O, heat (d) LiAlH4, then H₂Oarrow_forwardDraw the stepwise mechanism for the reactionsarrow_forwardDraw stepwise mechanismarrow_forward
- Part I. Draw reaction mechanism for the transformations of benzophenone to benzopinacol to benzopinaco lone and answer the ff: a) Give the major reason for the exposure of benzophenone al isopropyl alcohol (w/acid) to direct sunlight of pina colone Mechanism For b) Pinacol (2,3-dimethy 1, 1-3-butanediol) on treatment w/ acid gives a mixture (3,3-dimethyl-2-butanone) and 2, 3-dimethyl-1,3-butadiene. Give reasonable the formation of the productsarrow_forwardwhat are the Iupac names for each structurearrow_forwardWhat are the IUPAC Names of all the compounds in the picture?arrow_forward
- 1) a) Give the dominant Intermolecular Force (IMF) in a sample of each of the following compounds. Please show your work. (8) SF2, CH,OH, C₂H₂ b) Based on your answers given above, list the compounds in order of their Boiling Point from low to high. (8)arrow_forward19.78 Write the products of the following sequences of reactions. Refer to your reaction road- maps to see how the combined reactions allow you to "navigate" between the different functional groups. Note that you will need your old Chapters 6-11 and Chapters 15-18 roadmaps along with your new Chapter 19 roadmap for these. (a) 1. BHS 2. H₂O₂ 3. H₂CrO4 4. SOCI₂ (b) 1. Cl₂/hv 2. KOLBU 3. H₂O, catalytic H₂SO4 4. H₂CrO4 Reaction Roadmap An alkene 5. EtOH 6.0.5 Equiv. NaOEt/EtOH 7. Mild H₂O An alkane 1.0 2. (CH3)₂S 3. H₂CrO (d) (c) 4. Excess EtOH, catalytic H₂SO OH 4. Mild H₂O* 5.0.5 Equiv. NaOEt/EtOH An alkene 6. Mild H₂O* A carboxylic acid 7. Mild H₂O* 1. SOC₁₂ 2. EtOH 3.0.5 Equiv. NaOEt/E:OH 5.1.0 Equiv. NaOEt 6. NH₂ (e) 1. 0.5 Equiv. NaOEt/EtOH 2. Mild H₂O* Br (f) i H An aldehyde 1. Catalytic NaOE/EtOH 2. H₂O*, heat 3. (CH,CH₂)₂Culi 4. Mild H₂O* 5.1.0 Equiv. LDA Br An ester 4. NaOH, H₂O 5. Mild H₂O* 6. Heat 7. MgBr 8. Mild H₂O* 7. Mild H₂O+arrow_forwardLi+ is a hard acid. With this in mind, which if the following compounds should be most soluble in water? Group of answer choices LiBr LiI LiF LiClarrow_forward
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