Concept explainers
(a)
Interpretation:
Synthesis method of the given compound has to be given from the compound which have the same number of carbon atoms.
Concept Introduction:
Addition of water to
Under acidic conditions, alkyne reacts with water to produce an enol which then immediately converts into
The formed enol and ketone are called keto-enol tautomers.
Tautomerization: It is the process of inter conversion of tautomers and therefore the process can also be called as keto-enol tautomerization.
Hydroboration reaction:
It is the reaction in which an internal alkyne is converted into ketone. The reagents used for the hydroboration oxidation reaction is either
(b)
Interpretation:
Synthesis method of the given compound has to be given from the compound which have the same number of carbon atoms.
Concept Introduction:
Addition of water to alkynes in presence of acid:
Under acidic conditions, alkyne reacts with water to produce an enol which then immediately converts into ketone. For terminal alkynes, there is a need of catalyst which is mercury.
The formed enol and ketone are called keto-enol tautomers.
Tautomerization: It is the process of inter conversion of tautomers and therefore the process can also be called as keto-enol tautomerization.
Hydroboration reaction:
It is the reaction in which an internal alkyne is converted into ketone. The reagents used for the hydroboration oxidation reaction is either
(c)
Interpretation:
Synthesis method of the given compound has to be given from the compound which have the same number of carbon atoms.
Concept Introduction:
Addition of water to alkynes in presence of acid:
Under acidic conditions, alkyne reacts with water to produce an enol which then immediately converts into ketone. For terminal alkynes, there is a need of catalyst which is mercury.
The formed enol and ketone are called keto-enol tautomers.
Tautomerization: It is the process of inter conversion of tautomers and therefore the process can also be called as keto-enol tautomerization.
Hydroboration reaction:
It is the reaction in which an internal alkyne is converted into ketone. The reagents used for the hydroboration oxidation reaction is either
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Chapter 7 Solutions
EBK ORGANIC CHEMISTRY
- Identify the missing organic reactants in the following reaction: X + Y H+ two steps Note: This chemical equation only focuses on the important organic molecules in the reaction. Additional inorganic or small-molecule reactants or products (like H2O) are not shown. In the drawing area below, draw the skeletal ("line") structures of the missing organic reactants X and Y. You may draw the structures in any arrangement that you like, so long as they aren't touching. Click and drag to start drawing a structure. Х :arrow_forwardDraw the mechanism of friedel-crafts acylation using acetyl chloride of m-Xylenearrow_forwardI need help naming these in IUPACarrow_forward
- H R Part: 1/2 :CI: is a/an electrophile Part 2 of 2 Draw the skeletal structure of the product(s) for the Lewis acid-base reaction. Include lone pairs and formal charges (if applicable) on the structures. 4-7: H ö- H Skip Part Check X :C1: $ % L Fi Click and drag to start drawing a structure. MacBook Pro & ㅁ x G 0: P Add or increase positive formal cha Save For Later Submit ©2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centearrow_forwardDraw the friedel-crafts acylation mechanism of m-Xylenearrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forward
- 1. Base on this experimental results, how do you know that the product which you are turning in is methyl 3-nitrobenzoate(meta substituted product ) rather than either of the other two products? 2. What observation suggests that at least a small amount of one or both of the other two isomers are in the mother liquor?arrow_forwardExplain Huckel's rule.arrow_forwardhere is my question can u help me please!arrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning
- Introductory Chemistry: A FoundationChemistryISBN:9781337399425Author:Steven S. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub CoWorld of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning
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