Calculate the theoretical mass of acetanilide produced when the mass of aniline used in the reaction equates to 4.000g. The reaction goes 100% to completion and aniline is the limiting reagent

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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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4. Calculate the theoretical mass of acetanilide produced when the mass of aniline used in the reaction equates to 4.000g. The reaction goes 100% to completion and aniline is the limiting reagent
**Transcription for Educational Website:**

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**Experiment Details:**

**1. Catalyst Identification:**
Identify (name) the catalyst in the reaction for the synthesis of aspirin performed in our lab experiment.

**2. Limiting Reagent Definition:**
Define "limiting reagent" with respect to chemical reactions. Generate an APA style citation for the source/reference used. Reference: [APA Citation Online Resource](https://www.mun.ca/writingcentre/resources/modelpapers/csme2900explain/Presentations/WritingCitations-APA.pdf)

**3. Error Analysis and Suggestions:**
List the possible errors and your suggestion(s) to improve the synthesis of aspirin. Include the significance of your percent yield and melting point in this context. If needed, use more space by writing on the back.

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**Chemical Reaction Details:**

**4. Production of Acetanilide:**

The production of acetanilide involves the treatment of aniline with acetic anhydride, producing an amide called acetanilide and acetic acid as a byproduct. The reaction proceeds as follows:

**Chemical Equation:**

- **Reactants:**
  - Aniline (C₆H₇N)
    - Molar Mass: 93.13 g/mol
  - Acetic Anhydride (C₄H₆O₃)
    - Molar Mass: 102.09 g/mol

- **Products:**
  - Acetanilide (C₈H₉NO)
    - Molar Mass: 135.16 g/mol
  - Acetic Acid (C₂H₄O₂)
    - Molar Mass: 60.05 g/mol

**Instructions:**

Calculate the theoretical mass of acetanilide produced when 4,000 grams of aniline is used. Conversion from milliliters to grams will be necessary for liquids.

**Structural Formulas:**

- Aniline is shown with a benzene ring attached to an NH₂ group.
- Acetic anhydride is depicted with two carbonyl groups (C=O) flanking an oxygen atom, with CH₃ groups attached.
- Acetanilide consists of a benzene ring linked to an amide group (NHCOCH₃).

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Focus on understanding the chemical process and how to calculate theoretical yields based on stoichiometry.
Transcribed Image Text:**Transcription for Educational Website:** --- **Experiment Details:** **1. Catalyst Identification:** Identify (name) the catalyst in the reaction for the synthesis of aspirin performed in our lab experiment. **2. Limiting Reagent Definition:** Define "limiting reagent" with respect to chemical reactions. Generate an APA style citation for the source/reference used. Reference: [APA Citation Online Resource](https://www.mun.ca/writingcentre/resources/modelpapers/csme2900explain/Presentations/WritingCitations-APA.pdf) **3. Error Analysis and Suggestions:** List the possible errors and your suggestion(s) to improve the synthesis of aspirin. Include the significance of your percent yield and melting point in this context. If needed, use more space by writing on the back. --- **Chemical Reaction Details:** **4. Production of Acetanilide:** The production of acetanilide involves the treatment of aniline with acetic anhydride, producing an amide called acetanilide and acetic acid as a byproduct. The reaction proceeds as follows: **Chemical Equation:** - **Reactants:** - Aniline (C₆H₇N) - Molar Mass: 93.13 g/mol - Acetic Anhydride (C₄H₆O₃) - Molar Mass: 102.09 g/mol - **Products:** - Acetanilide (C₈H₉NO) - Molar Mass: 135.16 g/mol - Acetic Acid (C₂H₄O₂) - Molar Mass: 60.05 g/mol **Instructions:** Calculate the theoretical mass of acetanilide produced when 4,000 grams of aniline is used. Conversion from milliliters to grams will be necessary for liquids. **Structural Formulas:** - Aniline is shown with a benzene ring attached to an NH₂ group. - Acetic anhydride is depicted with two carbonyl groups (C=O) flanking an oxygen atom, with CH₃ groups attached. - Acetanilide consists of a benzene ring linked to an amide group (NHCOCH₃). --- Focus on understanding the chemical process and how to calculate theoretical yields based on stoichiometry.
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