
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

Want to see the full answer?
Check out a sample textbook solution
Chapter 7 Solutions
Organic Chemistry (8th Edition)
- Which of the following molecules are NOT typical carbohydrates? For the molecules that are carbohydrates, label them as an aldose or ketose. HO Он ОН ОН Он ОН но ΤΗ HO ОН HO eve Он он ОН ОН ОН If polyethylene has an average molecular weight of 25,000 g/mol, how many repeat units are present?arrow_forwardDraw the a-anomer cyclized pyranose Haworth projection of the below hexose. Circle the anomeric carbons. Number the carbons on the Fischer and Haworth projections. Assign R and S for each chiral center. HO CHO -H HO -H H- -OH H -OH CH₂OH Draw the ẞ-anomer cyclized furanose Haworth projection for the below hexose. Circle the anomeric carbons. Number the carbons on the Fischer and Haworth projections. HO CHO -H H -OH HO -H H -OH CH₂OHarrow_forwardName the below disaccharide. Circle any hemiacetals. Identify the numbering of glycosidic linkage, and identify it as a or ẞ. OH HO HO OH HO HO HO OHarrow_forward
- What are the monomers used to make the following polymers? F. а. b. с. d. Вецер хочому なarrow_forward1. Propose a reasonable mechanism for the following transformation. I'm looking for curved mechanistic arrows and appropriate formal charges on intermediates. OMe MeO OMe Me2N NMe2 OTBS OH xylenes OMe 'OTBSarrow_forwardWhat is the polymer made from the following monomers? What type of polymerization is used for each? а. ОН H2N но b. ن -NH2 d. H₂N NH2 довarrow_forward
- Condensation polymers are produced when monomers containing two different functional groups link together with the loss of a small molecule such as H2O. The difunctional monomer H2N(CH2)6COOH forms a condensation polymer. Draw the carbon-skeleton structure of the dimer that forms from this monomer.arrow_forwardWhat is the structure of the monomer?arrow_forward→ BINDERIYA GANBO... BINDERIYA GANBO. AP Biology Notes Gamino acid chart - G... 36:22 司 10 ☐ Mark for Review Q 1 Hide 80 8 2 =HA O=A¯ = H₂O Acid HIO HBrO HCIO Question 10 of 35 ^ Σ DELL □ 3 % Λ & 6 7 * ∞ 8 do 5 $ 4 # m 3 ° ( 9 Highlights & Notes AXC Sign out Carrow_forward
- Which representation(s) show polymer structures that are likely to result in rigid, hard materials and those that are likely to result in flexible, stretchable, soft materials?arrow_forward3. Enter the molecular weight of the product obtained from the Williamson Ether Synthesis? OH OH & OH excess CH3l Ag₂Oarrow_forwardPlease answer 1, 2 and 3 on the endarrow_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




