
(a)
To determine: The dehydrohalogenation product that results if the given
Interpretation: The dehydrohalogenation product that results if the given alkyl halide is heated in alcoholic
Concept introduction: The
The bimolecular elimination reaction that favours the removal of an HX substituent from an alkyl halide that needs a base to remove
The elimination of hydrogen halide molecule is termed as dehydrohalogenation. This type of reaction has an unfavourable enthalpy change but a favourable entropy change.
(b)
To determine: The dehydrohalogenation product that results if the given alkyl halide is heated in alcoholic
Interpretation: The dehydrohalogenation product that results if the given alkyl halide is heated in alcoholic
Concept introduction: The chemical reaction that consists of an alkyl halide, a good leaving group that reacts with Lewis base to form an alkene is termed as elimination reaction. In this reaction there is complete removal of the leaving group without any substitution.
The bimolecular elimination reaction that favours the removal of an HX substituent from an alkyl halide that needs a base to remove
The elimination of hydrogen halide molecule is termed as dehydrohalogenation. This type of reaction has an unfavourable enthalpy change but a favourable entropy change.
(c)
To determine: The dehydrohalogenation product that results if the given alkyl halide is heated in alcoholic
Interpretation: The dehydrohalogenation product that results if the given alkyl halide is heated in alcoholic
Concept introduction: The chemical reaction that consists of an alkyl halide, a good leaving group that reacts with Lewis base to form an alkene is termed as elimination reaction. In this reaction there is complete removal of the leaving group without any substitution.
The bimolecular elimination reaction that favours the removal of an HX substituent from an alkyl halide that needs a base to remove
The elimination of hydrogen halide molecule is termed as dehydrohalogenation. This type of reaction has an unfavourable enthalpy change but a favourable entropy change.
(d)
To determine: The dehydrohalogenation product that results if the given alkyl halide is heated in alcoholic
Interpretation: The dehydrohalogenation product that results if the given alkyl halide is heated in alcoholic
Concept introduction: The chemical reaction that consists of an alkyl halide, a good leaving group that reacts with Lewis base to form an alkene is termed as elimination reaction. In this reaction there is complete removal of the leaving group without any substitution.
The bimolecular elimination reaction that favours the removal of an HX substituent from an alkyl halide that needs a base to remove
The elimination of hydrogen halide molecule is termed as dehydrohalogenation. This type of reaction has an unfavourable enthalpy change but a favourable entropy change.
(e)
To determine: The dehydrohalogenation product that results if the given alkyl halide is heated in alcoholic
Interpretation: The dehydrohalogenation product that results if the given alkyl halide is heated in alcoholic
Concept introduction: The chemical reaction that consists of an alkyl halide, a good leaving group that reacts with Lewis base to form an alkene is termed as elimination reaction. In this reaction there is complete removal of the leaving group without any substitution.
The bimolecular elimination reaction that favours the removal of an HX substituent from an alkyl halide that needs a base to remove
The elimination of hydrogen halide molecule is termed as dehydrohalogenation. This type of reaction has an unfavourable enthalpy change but a favourable entropy change.
(f)
To determine: The dehydrohalogenation product that results if the given alkyl halide is heated in alcoholic
Interpretation: The dehydrohalogenation product that results if the given alkyl halide is heated in alcoholic
Concept introduction: The chemical reaction that consists of an alkyl halide, a good leaving group that reacts with Lewis base to form an alkene is termed as elimination reaction. In this reaction there is complete removal of the leaving group without any substitution.
The bimolecular elimination reaction that favours the removal of an HX substituent from an alkyl halide that needs a base to remove
The elimination of hydrogen halide molecule is termed as dehydrohalogenation. This type of reaction has an unfavourable enthalpy change but a favourable entropy change.

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Chapter 7 Solutions
Student's Solutions Manual for Organic Chemistry
- 4. 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_forward2. Provide reagents/conditions to accomplish the following syntheses. More than one step is required in some cases. a. CH3arrow_forward
- Identify 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_forwardInstructions: 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_forward
- a. H3C CH3 H, 1.0 equiv. Br2arrow_forwardH3C. H3C CH 3 CH 3 CH3 1. LDA 2. PhSeCl 3. H2O2arrow_forwardPlease predict the products for each of the following reactions: 1.03 2. H₂O NaNH, 1. n-BuLi 2. Mel A H₂ 10 9 0 H2SO4, H₂O HgSO4 Pd or Pt (catalyst) B 9 2 n-BuLi ♡ D2 (deuterium) Lindlar's Catalyst 1. NaNH2 2. EtBr Na, ND3 (deuterium) 2. H₂O2, NaOH 1. (Sia)2BH с Darrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning

