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(a)
Interpretation:
Reagents should be predicted for the given transformations.
Concept introduction:
Reagent: reagent is a compound or compound mixture that is used in the chemical transformation of the reactions. Reagents for some reactions are given below.
- Elimination reaction: in elimination reaction, two substituents are removed from the substrate to give the product in presence of base.
- Elimination of compound in presence of bulky base leads to less substituted
alkene , in presence of strong base (not bulky) leads to more substituted alkene. - Addition reaction: in addition reaction, two substituents are added to the reactant without losing any compound.
- Hydration: addition of water molecule across the double bond is called hydration reaction. Hydration of alkene can be achieved in many ways.
- Oxy mercuration-demercuration: this process undergoes through the addition of water according to Markovnikov’s rule without forming carbocation as intermediate.
- Hydroboration-oxidation reaction: addition of –H and –OH group across the double bond in presence of borane and hydrogen peroxide with base is known as hydroboration-oxidation reaction.
- Simple hydration in acidic media gives the addition product through carbocation intermediate.
- Hydro halogenation: hydrogen and halogen added across the double bond of the alkene in Markovnikov’s path is called hydro halogenation. This addition reaction proceeds via anti-Markovnikov’s path in presence of peroxides.
To find: the reagent for the given transformation.
(b)
Interpretation:
Reagents should be predicted for the given transformations.
Concept introduction:
Reagent: reagent is a compound or compound mixture that is used in the chemical transformation of the reactions. Reagents for some reactions are given below.
- Elimination reaction: in elimination reaction, two substituents are removed from the substrate to give the product in presence of base.
- Elimination of compound in presence of bulky base leads to less substituted alkene, in presence of strong base (not bulky) leads to more substituted alkene.
- Addition reaction: in addition reaction, two substituents are added to the reactant without losing any compound.
- Hydration: addition of water molecule across the double bond is called hydration reaction. Hydration of alkene can be achieved in many ways.
- Oxy mercuration-demercuration: this process undergoes through the addition of water according to Markovnikov’s rule without forming carbocation as intermediate.
- Hydroboration-oxidation reaction: addition of –H and –OH group across the double bond in presence of borane and hydrogen peroxide with base is known as hydroboration-oxidation reaction.
- Simple hydration in acidic media gives the addition product through carbocation intermediate.
- Hydro halogenation: hydrogen and halogen added across the double bond of the alkene in Markovnikov’s path is called hydro halogenation. This addition reaction proceeds via anti-Markovnikov’s path in presence of peroxides.
To find: the reagent for the given transformation.
(c)
Interpretation:
Reagents should be predicted for the given transformations.
Concept introduction:
Reagent: reagent is a compound or compound mixture that is used in the chemical transformation of the reactions. Reagents for some reactions are given below.
- Elimination reaction: in elimination reaction, two substituents are removed from the substrate to give the product in presence of base.
- Elimination of compound in presence of bulky base leads to less substituted alkene, in presence of strong base (not bulky) leads to more substituted alkene.
- Addition reaction: in addition reaction, two substituents are added to the reactant without losing any compound.
- Hydration: addition of water molecule across the double bond is called hydration reaction. Hydration of alkene can be achieved in many ways.
- Oxy mercuration-demercuration: this process undergoes through the addition of water according to Markovnikov’s rule without forming carbocation as intermediate.
- Hydroboration-oxidation reaction: addition of –H and –OH group across the double bond in presence of borane and hydrogen peroxide with base is known as hydroboration-oxidation reaction.
- Simple hydration in acidic media gives the addition product through carbocation intermediate.
- Hydro halogenation: hydrogen and halogen added across the double bond of the alkene in Markovnikov’s path is called hydro halogenation. This addition reaction proceeds via anti-Markovnikov’s path in presence of peroxides.
To find: the reagent for the given transformation.
(d)
Interpretation:
Reagents should be predicted for the given transformations.
Concept introduction:
Reagent: reagent is a compound or compound mixture that is used in the chemical transformation of the reactions. Reagents for some reactions are given below.
- Elimination reaction: in elimination reaction, two substituents are removed from the substrate to give the product in presence of base.
- Elimination of compound in presence of bulky base leads to less substituted alkene, in presence of strong base (not bulky) leads to more substituted alkene.
- Addition reaction: in addition reaction, two substituents are added to the reactant without losing any compound.
- Hydration: addition of water molecule across the double bond is called hydration reaction. Hydration of alkene can be achieved in many ways.
- Oxy mercuration-demercuration: this process undergoes through the addition of water according to Markovnikov’s rule without forming carbocation as intermediate.
- Hydroboration-oxidation reaction: addition of –H and –OH group across the double bond in presence of borane and hydrogen peroxide with base is known as hydroboration-oxidation reaction.
- Simple hydration in acidic media gives the addition product through carbocation intermediate.
- Hydro halogenation: hydrogen and halogen added across the double bond of the alkene in Markovnikov’s path is called hydro halogenation. This addition reaction proceeds via anti-Markovnikov’s path in presence of peroxides.
To find: the reagent for the given transformation.
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Chapter 9 Solutions
Student Study Guide and Solutions Manual T/A Organic Chemistry
- #1. Retro-Electrochemical Reaction: A ring has been made, but the light is causing the molecule to un- cyclize. Undo the ring into all possible molecules. (2pts, no partial credit) hvarrow_forwardDon't used Ai solutionarrow_forwardI have a question about this problem involving mechanisms and drawing curved arrows for acids and bases. I know we need to identify the nucleophile and electrophile, but are there different types of reactions? For instance, what about Grignard reagents and other types that I might not be familiar with? Can you help me with this? I want to identify the names of the mechanisms for problems 1-14, such as Gilman reagents and others. Are they all the same? Also, could you rewrite it so I can better understand? The handwriting is pretty cluttered. Additionally, I need to label the nucleophile and electrophile, but my main concern is whether those reactions differ, like the "Brønsted-Lowry acid-base mechanism, Lewis acid-base mechanism, acid-catalyzed mechanisms, acid-catalyzed reactions, base-catalyzed reactions, nucleophilic substitution mechanisms (SN1 and SN2), elimination reactions (E1 and E2), organometallic mechanisms, and so forth."arrow_forward
- 2. 200 LOD For an unknown compound with a molecular ion of 101 m/z: a. Use the molecular ion to propose at least two molecular formulas. (show your work) b. What is the DU for each of your possible formulas? (show your work) C. Solve the structure and assign each of the following spectra. 8 6 4 2 (ppm) 150 100 50 ō (ppm) 4000 3000 2000 1500 1000 500 HAVENUMBERI-11arrow_forwardComplete the spectroscopy with structurearrow_forwardComplete the spectroscopy with structurearrow_forward
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