Organic Chemistry Plus Masteringchemistry With Pearson Etext, Global Edition
9th Edition
ISBN: 9781292151229
Author: Wade, LeRoy G.
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Textbook Question
Chapter 9, Problem 9.36SP
Predict the products formed when CH3CH2—C ≡ C :− Na+ reacts with the following compounds.
- a. ethyl bromide
- b. tert-butyl bromide
- c. formaldehyde
- d. cyclohexanone
- 1. e CH3CH2CH2CHO
- e. cyclohexanol
- f. butan-2-one, CH3CH2COCH3
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
What product(s) will form:
2-Pentene + H₂O →
O a.
2-Pentanol
O b. Isopropyl alcohol
O c. 3-Pentanol
O d. a 50/50 mixture of 2-Pentanol and 3-Pentanol
Oe. no reaction will occur
Pd/C, H2
a. Propylcyclohexane
O b. Propylbenzene
OC. Benzoic acid
O d.1-propenyl cyclohexane
From the given two compounds in the image, which reagents would differentiate the pair?
a. Br2 in CH2Cl2
b. CrO3, H2SO4, acetone
c. concentrated HCl with ZnCl2
d. aqueous FeCl3
e. aqueous NAHCO3
f. ammoniacal AgNo3
Chapter 9 Solutions
Organic Chemistry Plus Masteringchemistry With Pearson Etext, Global Edition
Ch. 9.1 - a. Count the elements of unsaturation in...Ch. 9.2 - Prob. 9.2PCh. 9.4B - What reaction would acetylene likely undergo if it...Ch. 9.6 - Prob. 9.4PCh. 9.6 - Predict the products of the following acid-base...Ch. 9.7A - Solved Problem9-1 showed the synthesis of...Ch. 9.7A - Show how you might synthesize the following...Ch. 9.7B - Prob. 9.8PCh. 9.7B - Show how you would synthesize...Ch. 9.8 - When 2,2-dibromo-1-phenylpropane is heated...
Ch. 9.8 - When 2,2-dibromo-1-phenylpropane is heated...Ch. 9.9C - Show how you would convert a. oct-3-yne to...Ch. 9.9C - The fragrance of (Z)-1-phenylhex-2-en-1-ol...Ch. 9.9D - In the addition of just 1 mole of bromine to 1...Ch. 9.9E - Propose a mechanism for the entire reaction of...Ch. 9.9E - Predict the major product(s) of the following...Ch. 9.9E - Propose a mechanism for the reaction of pent-1-yne...Ch. 9.9E - Show how hex-1-yne might be converted to a....Ch. 9.9F - When pent-2-yne reacts with mercuric sulfate in...Ch. 9.9F - Prob. 9.20PCh. 9.9F - Prob. 9.21PCh. 9.9F - Prob. 9.22PCh. 9.10A - Predict the product(s) you would expect from...Ch. 9.10B - Prob. 9.24PCh. 9.10B - Prob. 9.25PCh. 9 - Prob. 9.26SPCh. 9 - Give common names for the following compounds. a....Ch. 9 - Prob. 9.28SPCh. 9 - Prob. 9.29SPCh. 9 - Using cyclooctyne as your starting material, show...Ch. 9 - Prob. 9.31SPCh. 9 - Prob. 9.32SPCh. 9 - Predict the products of reaction of pent-1-yne...Ch. 9 - Show how you would accomplish the following...Ch. 9 - Show how you would synthesize the following...Ch. 9 - Predict the products formed when CH3CH2C C : Na+...Ch. 9 - Prob. 9.37SPCh. 9 - Prob. 9.38SPCh. 9 - When compound Z is treated with ozone, followed by...Ch. 9 - Show how you would convert the following starting...Ch. 9 - The following functional-group interchange is a...Ch. 9 - Using any necessary inorganic reagents, show how...Ch. 9 - Prob. 9.43SP
Additional Science Textbook Solutions
Find more solutions based on key concepts
Give one example from main group chemistry that illustrates each of the following descriptions: (a) Covalent ne...
General Chemistry: Atoms First
For each of the following 2-dimensional shapes, determine the highest order rotation axis of symmetry.
Inorganic Chemistry
The chapter sections to review are shown in parentheses at the end of each problem. A "chemical-free” shampoo i...
Basic Chemistry
Q1. What is the empirical formula of a compound with the molecular formula
Chemistry: A Molecular Approach
Draw a Lewis structure for each of the following species: a. H2CO3 b. CO32 c. CH2O d. CO2
Essential Organic Chemistry (3rd Edition)
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- identify the product formed in the following S№² reaction: § 2 OH A. Br H₂0 Br acetone میں B. سه C. OH ||| D. OHarrow_forwardQUESTION 2 The following is a proposed synthetic strategy that uses one starting alcohol in two separate single-step reactions (I and II) to make a pair of diene and dienophile which together undergo a Diels-Alder reaction to give a Diels-Alder product. The Diels-Alder product is subsequently converted to the final ether in a three-step synthesis (III, IV and V). Identify the reagent(s) from Table I required for each of those three sysnthese and place the number (A1, A2 reagent(s) in the given box right next to the corresponding step numbers (I to V) of the synthesis. DO NOT fill in any box with more than one number. (Note: This question is different from the previous synthesis question which allows two numbers for each box). You will be graded based on the number in each box. Do not fill in any single box with more than one number. Do not leave any box blank. B1, B2..., or C1, C2 ...) that represents the (I) diene OH (III, IV and V) Diesl-Alder product (II) dienophile Table I Number…arrow_forward40. Deuterium oxide, D20, is water that contains the stable hydrogen isotope 2H, usually shown as D. When dissolved in deuterium oxide, ethanol undergoes the following reaction: * CH3CH2OH + D½0 → CH;CH2OD + HOD What is the best way of showing that this reaction has occurred? A. By testing the product with phosphorus pentachloride and not getting steamy fumes. B. By determining the mass spectrum of the mixture and showing peaks at m/z values of 20 and 46. C. By fractionally distilling the mixture and determining the amount of CH3CH2OD using a Geiger counter. D. By determining the mass spectrum of the mixture and showing peaks at m/z values by 19 and 47. A В O Darrow_forward
- B. Draw structures for the products in the following reactions. my NH₂ NH₂ 1. LIAIH4 2. H₂O* xs EtBr 1. Mel 2. Ag₂O, H,O, heat acetone, formaldehyde cat. HCIarrow_forwardQuestion 18.c of 20 Aldehydes and ketones are common carbonyl functional groups. Identify the structures and provide names of these molecules. Provide a systematic name for this structure. سکتے 5- H 1- 4- cyclo tert- 6- di n- tri 3- 2- sec- hex eth but Submit +arrow_forwardWhat is the organic product? столосно NaOC₂H₂ H+ + CH-CH-C-OCHS CH+CH.C HOC₂H5 CH3 III. I. C₂H₂O CH O II. CH3-C CH3 CH-CH-C--OC₂H CH3 OH C₂H₂OCH CH O CH3-C-C-OC₂HS CH3 IV. C₂H₂O 0 CH3-C-C-OC₂HS CH3arrow_forward
- 2. What type of chemical reaction is illustrated by the following reaction? CH3OOCH3 + H2O ⎯→ CH3OOH + CH3OH a. oxidation/reduction b. substitution c. neutralization d. hydrolysis e. dehydration synthesis (condensation)arrow_forwardChoose the correct product for the given reaction. CF3 HBr ? CF3 CF3 Br A. Br Br CF3 Br CF3 D. Br С. Br A B B. ооо оarrow_forwardWhat is the product of the following reaction? A. B. شما NH NH2Et, cat H* C. ZI avant HO. D. `N OHarrow_forward
- 1l Normal l No Spac. A-空,A. KJIDPAL U - abx X, Paragraph Font Easter makes unique smells: 2-methyl-2-butanol + acetic acid →> 3-methyl-2-butanol + acetic acid –> 1-propanol + acetic acid –> 1-Octanol + acetic acid -> 2-methyl - propanol + formic acid acetic acid –> LA English (United States) to searcharrow_forwardReagents a. CeHsCHO b. NaOH, ethanol c. Pyrrolidine, cat. H* d. H2C=CHCN e. H30* f. LDA g. ELOC(=0)CO,Et h. BRCH2CH=CH2 Na* OEt, ethanol j. Br2, H* k. K* t-BuO 1. CH2(CO2Et)2 m. heat Select reagents from the table to synthesize this compound from cyclopentanone. Enter the letters of the chosen reagents, in the order that you wish to use them, without spaces or punctuation (i.e. geda). Submit Answer Try Another Version 1 Item attempt remainingarrow_forward1. For the following reaction, OEt ethyl 2-phenylacetate C10H12O2 164.20 g/mol 1. NaOEt 2. H3O+ алд OEt ethyl 3-oxo-2,4-diphenylbutanoate C18H1803 282.34 g/mol b. What is the theoretical yield, using the amounts given in part a? c. What is the percent yield if 0.328 g of product are isolated? EtOH a. What is the limiting reagent when 0.495 g of ethyl 2-phenylacetate is combined with 1.20 g of sodium ethoxide (NaOEt, 68.05 g/mol)? ethanol C₂H6O 46.07 g/molarrow_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 LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples 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 EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary 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
Chapter 4 Alkanes and Cycloalkanes Lesson 2; Author: Linda Hanson;https://www.youtube.com/watch?v=AL_CM_Btef4;License: Standard YouTube License, CC-BY
Chapter 4 Alkanes and Cycloalkanes Lesson 1; Author: Linda Hanson;https://www.youtube.com/watch?v=PPIa6EHJMJw;License: Standard Youtube License