![ORGANIC CHEMISTRY-WILEYPLUS NEXTGEN](https://www.bartleby.com/isbn_cover_images/9781119760924/9781119760924_largeCoverImage.gif)
ORGANIC CHEMISTRY-WILEYPLUS NEXTGEN
4th Edition
ISBN: 9781119760924
Author: Klein
Publisher: WILEY
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 12, Problem 54ASP
Interpretation Introduction
Interpretation:
The compound which does not give
Concept introduction:
When a Grignard reagent reacts with a carbonyl compound, the alkyl part of the reagent acts as a nucleophile and attacks the electrophilic carbonyl carbon, forming an intermediate compound. This after an acidic aqueous workup yields the product, generally alcohol, depending on the starting carbonyl compound used. The basicity of the Grignard reagent plays an important role in the kinetics and yield of the reaction.
Expert Solution & Answer
![Check Mark](/static/check-mark.png)
Want to see the full answer?
Check out a sample textbook solution![Blurred answer](/static/blurred-answer.jpg)
Students have asked these similar questions
CH3
OCH2CH2CH CH3
(10)
(11)
alkyl bromide/
phenyl bromide
sodium alkoxide/
sodium phenoxide
Provide a primary organic product(s) for each reaction shown and a proper IUPAC name
7.
OCH3
What is the IUPAC name of the compound in the image?
5-butyl-4-methoxyhept-3-ol
5-ethyl-3-hydroxy-4-methoxide
5-ethyl-4-methoxynonan-3-ol
5-ethyl-6-methoxynonan-7-ol
ОН
Chapter 12 Solutions
ORGANIC CHEMISTRY-WILEYPLUS NEXTGEN
Ch. 12.1 - Prob. 1LTSCh. 12.1 - Prob. 1PTSCh. 12.1 - Prob. 2ATSCh. 12.1 - Prob. 3CCCh. 12.2 - Prob. 4CCCh. 12.3 - Prob. 8CCCh. 12.3 - Prob. 9CCCh. 12.4 - Prob. 3LTSCh. 12.4 - Prob. 10PTSCh. 12.4 - Prob. 11ATS
Ch. 12.4 - Prob. 4LTSCh. 12.4 - Prob. 12PTSCh. 12.4 - Prob. 13ATSCh. 12.6 - Prob. 14CCCh. 12.6 - Prob. 5LTSCh. 12.6 - Prob. 15PTSCh. 12.6 - Prob. 16PTSCh. 12.7 - Prob. 18CCCh. 12.9 - Prob. 6LTSCh. 12.9 - Prob. 19PTSCh. 12.9 - Prob. 20ATSCh. 12.9 - Prob. 21CCCh. 12.10 - Prob. 7LTSCh. 12.10 - Prob. 22PTSCh. 12.10 - Prob. 23ATSCh. 12.13 - Prob. 8LTSCh. 12.13 - Prob. 24PTSCh. 12.13 - Prob. 25ATSCh. 12.13 - Prob. 26CCCh. 12.13 - Prob. 9LTSCh. 12.13 - Prob. 27PTSCh. 12.13 - Prob. 28ATSCh. 12 - Prob. 29PPCh. 12 - Prob. 30PPCh. 12 - Prob. 31PPCh. 12 - Prob. 32PPCh. 12 - Prob. 33PPCh. 12 - Prob. 34PPCh. 12 - Prob. 35PPCh. 12 - Prob. 36PPCh. 12 - Prob. 37PPCh. 12 - Prob. 38PPCh. 12 - Prob. 39PPCh. 12 - Prob. 40PPCh. 12 - Prob. 41PPCh. 12 - Prob. 42PPCh. 12 - Prob. 43PPCh. 12 - Prob. 44PPCh. 12 - Prob. 45PPCh. 12 - Prob. 46PPCh. 12 - Prob. 47PPCh. 12 - Prob. 48PPCh. 12 - Prob. 49PPCh. 12 - Prob. 50PPCh. 12 - Prob. 51PPCh. 12 - Prob. 52PPCh. 12 - Prob. 53ASPCh. 12 - Prob. 54ASPCh. 12 - Prob. 55ASPCh. 12 - Prob. 62IPCh. 12 - Prob. 64IPCh. 12 - Prob. 65IPCh. 12 - Prob. 66IPCh. 12 - Prob. 67IPCh. 12 - Prob. 68IPCh. 12 - Prob. 69IPCh. 12 - Prob. 74IP
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
- Ochem IUPAC names Can you please see if I have named these correctly (see the attached image for the compound structures) I have them named as follows: 1-iodo-4-methoxy-2-nitrobenzene 3-bromo-5-phenylaniline 4-cyclopentyl-2-hydroxybenzoic acid 3-methyl-1-phenylbutan-1-ol If these are incorrect please correct them!arrow_forwardProvide the major organic product of the following reaction. but-1-ene H₂O, H+ What type of regiochemistry is observed in the major product of an acid catalyzed hydration reaction? A) Anti-addition B) Syn-addition C) anti-Markovnikov D) Markovnikovarrow_forwardNucleophilic carbon atoms are often important in the formation of carbon–carbon bonds. Carbon atoms are not good nucleophiles if they do not possess a lone pair of electrons.arrow_forward
- Provide the major organic product of the following reaction. CH3 HNO3, H₂SO4, Aarrow_forwardExplain why the C=C of an enol is more nucleophilic than the C=C of an alkene, despite the fact that the electronegative oxygen atom of the enol inductively withdraws electron density from the carbon–carbon double bond.arrow_forwardPick the best IUPAC name for the following molecule: H3C-O CH3 CH3 H3C- O 2,4,5-trimethylheptanal O5-methoxy-2,4-dimethylheptanoic Acid O 5-methoxy-2,4-dimethylheptanal 5-methoxy-2,4-dimethylheptan-1-olarrow_forward
- Provide the major organic product of the following reaction. but-1-yne 1) Sia₂BH 2) H₂O₂, OH What is it called when an enol converts to a keto? A) Keto-enol isomerism B) Keto-enol tater tot-ism C) Keto-enol conversion D) Keto-enol tautomerismarrow_forward5 AM 7.12. Draw the structural formula of the enol formed in each alkyne hydration reaction; then draw the structural formula of the carbonyl compound with which each enol is in equilibrium. (a) CH, (CH₂), C=CH + H₂O (b) CH, (CH₂),C=CH HgSO4 H₂SO4 1. (sia), BH 2. NaOH/H₂O₂ (an enol) → →(an enol) →arrow_forward16. Which of the following compounds reacts most rapidly with HNO3/H₂SO4? A) toluene B) anisole C) nitrobenzene D) fluorobenzenearrow_forward
- Give the IUPAC name for each compound (a)-(e)arrow_forwardOf the following structures, which is the most stable enol form?arrow_forwardIsotretinoin is a retinoid derivative of vitamin A used in the treatment of severe recalcitrant acne. What is the degree of substitution of the encircled alkene functional group in its structure? HO, A trisubstituted monosubstituted tetrasubstituted D disubstitutedarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningOrganic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305580350/9781305580350_smallCoverImage.gif)
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305080485/9781305080485_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9780618974122/9780618974122_smallCoverImage.gif)
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning
Alcohols, Ethers, and Epoxides: Crash Course Organic Chemistry #24; Author: Crash Course;https://www.youtube.com/watch?v=j04zMFwDeDU;License: Standard YouTube License, CC-BY