
(a)
Interpretation:
The synthesis of the given product transformation should be identified.
Concept introduction:
Bromination:
Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical.
Oxidation: Alcohols undergoing oxidation by using oxidizing agent like
9-BBN (9-Borabicyclo [3.3.1] nonane) or diborane is used for the hydroboration of
Sodium methoxide a strong base, which used for the abstraction the hydrogen from the molecule.
Grignard reaction: Organomagnesium halide (Grignard reagent) undergoes reaction with a ketone or
Hydrogenation: Molecular hydrogen (
(b)
Interpretation:
The synthesis of the given product transformation should be identified.
Concept introduction:
Bromination:
Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical. Alkanes undergo radical bromination by using
Oxidation: Alcohols undergoing oxidation by using oxidizing agent like
9-BBN (9-Borabicyclo [3.3.1] nonane) or diborane is used for the hydroboration of alkene. Boron addition to the double bond and subsequent oxidation of the new formed borane yields anti-Markovnikov alcohols
Sodium methoxide a strong base, which used for the abstraction the hydrogen from the molecule.
Grignard reaction: Organomagnesium halide (Grignard reagent) undergoes reaction with a ketone or aldehyde to form an alcohol
Hydrogenation: Molecular hydrogen (
(c)
Interpretation:
The synthesis of the given product transformation should be identified.
Concept introduction:
Bromination:
Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical. Alkanes undergo radical bromination by using
Oxidation: Alcohols undergoing oxidation by using oxidizing agent like
9-BBN (9-Borabicyclo [3.3.1] nonane) or diborane is used for the hydroboration of alkene. Boron addition to the double bond and subsequent oxidation of the new formed borane yields anti-Markovnikov alcohols
Sodium methoxide a strong base, which used for the abstraction the hydrogen from the molecule.
Grignard reaction: Organomagnesium halide (Grignard reagent) undergoes reaction with a ketone or aldehyde to form an alcohol
Hydrogenation: Molecular hydrogen (
(d)
Interpretation:
The synthesis of the given product transformation should be identified.
Concept introduction:
Bromination:
Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical. Alkanes undergo radical bromination by using
Oxidation: Alcohols undergoing oxidation by using oxidizing agent like
9-BBN (9-Borabicyclo [3.3.1] nonane) or diborane is used for the hydroboration of alkene. Boron addition to the double bond and subsequent oxidation of the new formed borane yields anti-Markovnikov alcohols
Sodium methoxide a strong base, which used for the abstraction the hydrogen from the molecule.
Grignard reaction: Organomagnesium halide (Grignard reagent) undergoes reaction with a ketone or aldehyde to form an alcohol
Hydrogenation: Molecular hydrogen (
(e)
Interpretation:
The synthesis of the given product transformation should be identified.
Concept introduction:
Bromination:
Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical. Alkanes undergo radical bromination by using
Oxidation: Alcohols undergoing oxidation by using oxidizing agent like
9-BBN (9-Borabicyclo [3.3.1] nonane) or diborane is used for the hydroboration of alkene. Boron addition to the double bond and subsequent oxidation of the new formed borane yields anti-Markovnikov alcohols
Sodium methoxide a strong base, which used for the abstraction the hydrogen from the molecule.
Grignard reaction: Organomagnesium halide (Grignard reagent) undergoes reaction with a ketone or aldehyde to form an alcohol
Hydrogenation: Molecular hydrogen (
(f)
Interpretation:
The synthesis of the given product transformation should be identified.
Concept introduction:
Bromination:
Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical. Alkanes undergo radical bromination by using
Oxidation: Alcohols undergoing oxidation by using oxidizing agent like
9-BBN (9-Borabicyclo [3.3.1] nonane) or diborane is used for the hydroboration of alkene. Boron addition to the double bond and subsequent oxidation of the new formed borane yields anti-Markovnikov alcohols
Sodium methoxide a strong base, which used for the abstraction the hydrogen from the molecule.
Grignard reaction: Organomagnesium halide (Grignard reagent) undergoes reaction with a ketone or aldehyde to form an alcohol
Hydrogenation: Molecular hydrogen (
(g)
Interpretation:
The synthesis of the given product transformation should be identified.
Concept introduction:
Bromination:
Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical. Alkanes undergo radical bromination by using
Oxidation: Alcohols undergoing oxidation by using oxidizing agent like
9-BBN (9-Borabicyclo [3.3.1] nonane) or diborane is used for the hydroboration of alkene. Boron addition to the double bond and subsequent oxidation of the new formed borane yields anti-Markovnikov alcohols
Sodium methoxide a strong base, which used for the abstraction the hydrogen from the molecule.
Grignard reaction: Organomagnesium halide (Grignard reagent) undergoes reaction with a ketone or aldehyde to form an alcohol
Hydrogenation: Molecular hydrogen (

Want to see the full answer?
Check out a sample textbook solution
Chapter 12 Solutions
Organic Chemistry
- 23.34 Show how to convert each starting material into isobutylamine in good yield. ཅ ནད ཀྱི (b) Br OEt (c) (d) (e) (f) Harrow_forwardPlease help me Please use https://app.molview.com/ to draw this. I tried, but I couldn't figure out how to do it.arrow_forwardPropose a synthesis of 1-butanamine from the following: (a) a chloroalkane of three carbons (b) a chloroalkane of four carbonsarrow_forward
- Select the stronger base from each pair of compounds. (a) H₂CNH₂ or EtzN (b) CI or NH2 NH2 (c) .Q or EtzN (d) or (e) N or (f) H or Harrow_forward4. Provide a clear arrow-pushing mechanism for each of the following reactions. Do not skip proton transfers, do not combine steps, and make sure your arrows are clear enough to be interpreted without ambiguity. a. 2. 1. LDA 3. H3O+ HOarrow_forwardb. H3C CH3 H3O+ ✓ H OHarrow_forward
- 2. Provide reagents/conditions to accomplish the following syntheses. More than one step is required in some cases. a. CH3arrow_forwardIdentify and provide an explanation that distinguishes a qualitative and quantitative chemical analysis. Provide examples.arrow_forwardIdentify and provide an explanation of the operational principles behind a Atomic Absorption Spectrometer (AAS). List the steps involved.arrow_forward
- Instructions: Complete the questions in the space provided. Show all your work 1. You are trying to determine the rate law expression for a reaction that you are completing at 25°C. You measure the initial reaction rate and the starting concentrations of the reactions for 4 trials. BrO³¯ (aq) + 5Br¯ (aq) + 6H* (aq) → 3Br₂ (l) + 3H2O (l) Initial rate Trial [BrO3] [H*] [Br] (mol/L) (mol/L) | (mol/L) (mol/L.s) 1 0.10 0.10 0.10 8.0 2 0.20 0.10 0.10 16 3 0.10 0.20 0.10 16 4 0.10 0.10 0.20 32 a. Based on the above data what is the rate law expression? b. Solve for the value of k (make sure to include proper units) 2. The proposed reaction mechanism is as follows: i. ii. BrО¸¯ (aq) + H+ (aq) → HBrO3 (aq) HBrO³ (aq) + H* (aq) → H₂BrO3* (aq) iii. H₂BrO³* (aq) + Br¯ (aq) → Br₂O₂ (aq) + H2O (l) [Fast] [Medium] [Slow] iv. Br₂O₂ (aq) + 4H*(aq) + 4Br(aq) → 3Br₂ (l) + H2O (l) [Fast] Evaluate the validity of this proposed reaction. Justify your answer.arrow_forwardе. Д CH3 D*, D20arrow_forwardC. NaOMe, Br Brarrow_forward
- 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





