A CI 1) ? H₂N & AICI3 2) HNO3 & H₂SO4 3) H₂ & Pd/C B 1) HNO3 & H₂SO4 CI 2) & AICI 3 3) H₂ & Pd/C с 1) HNO3 & H₂SO4 2) H₂ & Pd/C CI 3) & AICI 3 1) & AICI 3 2) Cl₂ & FeCl3 3) NH3

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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Which sequence of reactions would be best for achieving the transformation shown below?

The image depicts a chemical reaction problem where benzene is converted to a particular compound with certain substituents, specifically an amino group and an isopropyl group. The question mark indicates that the pathway or reagents needed to achieve this conversion must be determined. There are four possible options labeled A, B, C, and D, each detailing a sequence of reactions.

**Option A:**
1. React benzene with chloroethane (Cl) in the presence of AlCl₃ (Friedel-Crafts alkylation).
2. Nitrate the product using HNO₃ and H₂SO₄.
3. Reduce the nitro group using hydrogen (H₂) and palladium on carbon (Pd/C) as a catalyst.

**Option B:**
1. Nitrate benzene using HNO₃ and H₂SO₄.
2. React the product with chloroethane (Cl) in the presence of AlCl₃.
3. Reduce the nitro group using hydrogen (H₂) and palladium on carbon (Pd/C).

**Option C:**
1. Nitrate benzene using HNO₃ and H₂SO₄.
2. Reduce the nitro group using hydrogen (H₂) and palladium on carbon (Pd/C).
3. React with chloroethane (Cl) in the presence of AlCl₃.

**Option D:**
1. React benzene with chloroethane (Cl) in the presence of AlCl₃.
2. Chlorinate the product using Cl₂ in the presence of FeCl₃.
3. Treat with ammonia (NH₃).

The aim is to identify the correct sequence of reactions that will produce the indicated amino-isopropyl benzene from benzene.
Transcribed Image Text:The image depicts a chemical reaction problem where benzene is converted to a particular compound with certain substituents, specifically an amino group and an isopropyl group. The question mark indicates that the pathway or reagents needed to achieve this conversion must be determined. There are four possible options labeled A, B, C, and D, each detailing a sequence of reactions. **Option A:** 1. React benzene with chloroethane (Cl) in the presence of AlCl₃ (Friedel-Crafts alkylation). 2. Nitrate the product using HNO₃ and H₂SO₄. 3. Reduce the nitro group using hydrogen (H₂) and palladium on carbon (Pd/C) as a catalyst. **Option B:** 1. Nitrate benzene using HNO₃ and H₂SO₄. 2. React the product with chloroethane (Cl) in the presence of AlCl₃. 3. Reduce the nitro group using hydrogen (H₂) and palladium on carbon (Pd/C). **Option C:** 1. Nitrate benzene using HNO₃ and H₂SO₄. 2. Reduce the nitro group using hydrogen (H₂) and palladium on carbon (Pd/C). 3. React with chloroethane (Cl) in the presence of AlCl₃. **Option D:** 1. React benzene with chloroethane (Cl) in the presence of AlCl₃. 2. Chlorinate the product using Cl₂ in the presence of FeCl₃. 3. Treat with ammonia (NH₃). The aim is to identify the correct sequence of reactions that will produce the indicated amino-isopropyl benzene from benzene.
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