Homework Help is Here – Start Your Trial Now!
Science
Chemistry
1) Na, CH3OH A. o-Xylene 2) NH3 1) R2NH, H", - H20 B. Cycloheptanone 2) EtHC-CHCOEt 3) НО +

1) Na, CH3OH A. o-Xylene 2) NH3 1) R2NH, H", - H20 B. Cycloheptanone 2) EtHC-CHCOEt 3) НО +

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
See similar textbooks
icon
Related questions
Question
Give the organic Product structure and stereochemistry
**Chemical Reaction Processes** _A. o-Xylene_ **Reagents:** 1. Na, CH₃OH 2. NH₃ _B. Cycloheptanone_ **Reagents:** 1. R₂NH, H⁺, - H₂O 2. EtHC=CHCOEt 3. H₃O⁺ **Explanation:** **Section A: o-Xylene Reaction** This chemical reaction involves o-xylene as the starting material. The reagents used for this transformation are sodium (Na), methanol (CH₃OH), and ammonia (NH₃). The arrow indicates a multi-step reaction that undergoes certain changes in the presence of these reagents. **Section B: Cycloheptanone Reaction** This section describes a reaction involving cycloheptanone. The process requires multiple steps and a sequence of reagents: 1. R₂NH (a secondary amine), H⁺ (a proton/hydrogen ion), and the removal of water (H₂O). 2. EtHC=CHCOEt (ethyl vinyl ketone). 3. H₃O⁺ (hydronium ion) for final protonation. Both sections illustrate step-by-step transformations in organic chemistry involving complex reagents to achieve the desired product.
Transcribed Image Text:**Chemical Reaction Processes** _A. o-Xylene_ **Reagents:** 1. Na, CH₃OH 2. NH₃ _B. Cycloheptanone_ **Reagents:** 1. R₂NH, H⁺, - H₂O 2. EtHC=CHCOEt 3. H₃O⁺ **Explanation:** **Section A: o-Xylene Reaction** This chemical reaction involves o-xylene as the starting material. The reagents used for this transformation are sodium (Na), methanol (CH₃OH), and ammonia (NH₃). The arrow indicates a multi-step reaction that undergoes certain changes in the presence of these reagents. **Section B: Cycloheptanone Reaction** This section describes a reaction involving cycloheptanone. The process requires multiple steps and a sequence of reagents: 1. R₂NH (a secondary amine), H⁺ (a proton/hydrogen ion), and the removal of water (H₂O). 2. EtHC=CHCOEt (ethyl vinyl ketone). 3. H₃O⁺ (hydronium ion) for final protonation. Both sections illustrate step-by-step transformations in organic chemistry involving complex reagents to achieve the desired product.
### Reaction C The chemical reaction follows three steps with the starting compound Ethyl nitrosacetate (EtCOCH₂NO₂): 1. **Reagent**: KOH (Potassium hydroxide) 2. **Reagent**: PhHC-CHCOOMe 3. **Reagent**: H₃O⁺ (Acidic work-up, often indicating hydronium ion or aqueous acid) ### Reaction D Starting with **n-Valeraldehyde** and the reagent **(Ph₃)P-CHPh** (Triphenylphosphine benzylidine): **n-Valeraldehyde + (Ph₃)P-CHPh → Product** --- In both cases, the exact products are not specified in the image. * **Reaction C** implies a multi-step organic synthesis likely involving base catalysis (KOH), an intermediate reagent (PhHC-CHCOOMe), and then an acidic work-up (H₃O⁺). * **Reaction D** suggests a Wittig reaction, typically used in organic chemistry to form alkenes from aldehydes and ketones. Both reactions are indicative of complex organic synthesis involving key reagents and intermediates to transform given starting materials into desired end products.
Transcribed Image Text:### Reaction C The chemical reaction follows three steps with the starting compound Ethyl nitrosacetate (EtCOCH₂NO₂): 1. **Reagent**: KOH (Potassium hydroxide) 2. **Reagent**: PhHC-CHCOOMe 3. **Reagent**: H₃O⁺ (Acidic work-up, often indicating hydronium ion or aqueous acid) ### Reaction D Starting with **n-Valeraldehyde** and the reagent **(Ph₃)P-CHPh** (Triphenylphosphine benzylidine): **n-Valeraldehyde + (Ph₃)P-CHPh → Product** --- In both cases, the exact products are not specified in the image. * **Reaction C** implies a multi-step organic synthesis likely involving base catalysis (KOH), an intermediate reagent (PhHC-CHCOOMe), and then an acidic work-up (H₃O⁺). * **Reaction D** suggests a Wittig reaction, typically used in organic chemistry to form alkenes from aldehydes and ketones. Both reactions are indicative of complex organic synthesis involving key reagents and intermediates to transform given starting materials into desired end products.
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 2 steps with 1 images

SEE SOLUTIONCheck out a sample Q&A here
Blurred answer
Knowledge Booster
Organometallic Compounds of d-Block Elements
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.
Recommended textbooks for you
Chemistry
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
Chemistry
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
Principles of Instrumental Analysis
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9780078021558
Author:
Janice Gorzynski Smith Dr.
Publisher:
McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning
Elementary Principles of Chemical Processes, Bind…
Elementary Principles of Chemical Processes, Bind…
Chemistry
ISBN:
9781118431221
Author:
Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:
WILEY
SEE MORE TEXTBOOKS