If only a single step is required, select (none) from the drop down list. ÇI ? CH3CH2CH2C=CH CH3CH2CH2C=CH2 Reaction 1: Step 1: [ Step 2: ÇI ? CH;CH2CH2C=CH CH3CH2CH2ČCH3 Reaction 2: ČI
If only a single step is required, select (none) from the drop down list. ÇI ? CH3CH2CH2C=CH CH3CH2CH2C=CH2 Reaction 1: Step 1: [ Step 2: ÇI ? CH;CH2CH2C=CH CH3CH2CH2ČCH3 Reaction 2: ČI
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...
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Select reagents from the above table to carry out each of the following reactions.
If only a single step is required, select (none) from the drop down list.
![**Reagents Available:**
a. H₂O, H₂SO₄, HgSO₄
b. BH₃ then H₂O₂
c. NaNH₂
d. CH₃CH₂Br
e. HCl, ether
f. H₂, Lindlar catalyst
g. Li, NH₃ (liq)
h. CH₂I₂, Zn(Cu)
i. H₂, Pd/C
j. Br₂, CH₂Cl₂
**Instructions:**
Select reagents from the above table to carry out each of the following reactions. If only a single step is required, select (none) from the drop-down list.
**Reaction 1:**
\[ \text{CH}_3\text{CH}_2\text{CH}_2\text{C}\equiv\text{CH} \rightarrow \text{CH}_3\text{CH}_2\text{CH}_2\text{C}=\text{CH}_2 \]
- **Step 1:** [Dropdown Selection]
- **Step 2:** [Dropdown Selection]
**Reaction 2:**
\[ \text{CH}_3\text{CH}_2\text{CH}_2\text{C}\equiv\text{CH} \rightarrow \text{CH}_3\text{CH}_2\text{CH}_2\text{C}(\text{Cl})\text{H}_2\text{C}(\text{Cl}) \]
- **Step 1:** [Dropdown Selection]
- **Step 2:** [Dropdown Selection]
**Explanation of Chemistry Concepts:**
- **Reaction 1 Objective:** Conversion of an alkyne to an alkene.
- **Reaction 2 Objective:** Transformation of an alkyne to a fully halogenated alkane.
- **Reagent Details:**
- Lindlar catalyst is used for partial hydrogenation of alkynes to cis-alkenes.
- Pd/C with hydrogen is used for complete hydrogenation to alkanes.
- halogenation with Br₂ leads to the addition of halogens across double or triple bonds.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fd20000fd-c8aa-4301-a2c7-8913bd047299%2Ff1f92fc3-2627-4ad9-b324-6689d14ec0a7%2Fksxv13k_processed.png&w=3840&q=75)
Transcribed Image Text:**Reagents Available:**
a. H₂O, H₂SO₄, HgSO₄
b. BH₃ then H₂O₂
c. NaNH₂
d. CH₃CH₂Br
e. HCl, ether
f. H₂, Lindlar catalyst
g. Li, NH₃ (liq)
h. CH₂I₂, Zn(Cu)
i. H₂, Pd/C
j. Br₂, CH₂Cl₂
**Instructions:**
Select reagents from the above table to carry out each of the following reactions. If only a single step is required, select (none) from the drop-down list.
**Reaction 1:**
\[ \text{CH}_3\text{CH}_2\text{CH}_2\text{C}\equiv\text{CH} \rightarrow \text{CH}_3\text{CH}_2\text{CH}_2\text{C}=\text{CH}_2 \]
- **Step 1:** [Dropdown Selection]
- **Step 2:** [Dropdown Selection]
**Reaction 2:**
\[ \text{CH}_3\text{CH}_2\text{CH}_2\text{C}\equiv\text{CH} \rightarrow \text{CH}_3\text{CH}_2\text{CH}_2\text{C}(\text{Cl})\text{H}_2\text{C}(\text{Cl}) \]
- **Step 1:** [Dropdown Selection]
- **Step 2:** [Dropdown Selection]
**Explanation of Chemistry Concepts:**
- **Reaction 1 Objective:** Conversion of an alkyne to an alkene.
- **Reaction 2 Objective:** Transformation of an alkyne to a fully halogenated alkane.
- **Reagent Details:**
- Lindlar catalyst is used for partial hydrogenation of alkynes to cis-alkenes.
- Pd/C with hydrogen is used for complete hydrogenation to alkanes.
- halogenation with Br₂ leads to the addition of halogens across double or triple bonds.
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