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Carboxylic acid handouts 1. Predict the product of the following reactions and show a mechanism '...
Pericyclic Reactions 1. Predict the products of the following reactions and propose a mechanism that explains...
Pericyclic Reactions 1. Predict the products of the following reactions and propose a mechanism that explains it Me a heat OMCN heat 9. Ome =-COME HOY Y hest MeOC 2. Propose a synthesis of the following molecules using acetaldehyde as your only starting material 3. Propose a mechanism for the following transformations Meo,
For each of the following reactions, determine which ELIMINATION mechanism (E1 or 2) will occur. Alkyl...
For each of the following reactions, determine which ELIMINATION mechanism (E1 or 2) will occur. Alkyl Halide Substitution: Base Strength: Mechanism Type: 2° 3° Methyl Strong E1 1° Weak E2 Draw the mechanism that leads to ALL products for the reaction. Finally, underline the major product of the elimination reaction: NaOCH Challenge Problems: Synthesis: Predicted Ability: Good Average Poor Actual Ability: Good Average Poor Propose a synthesis from the starting material to obtain the indicated goal molecule. Note that any...
5. Predict the major organic products of the following reactions. Show all asymmetric carbons with wedgeldash...
5. Predict the major organic products of the following reactions. Show all asymmetric carbons with wedgeldash notation (i.e., as shown in the starting material). If a reaction produces a racemic mixture, show only one of the enantiomers produced. Carefully note the requested reaction mechanism for each reaction. (20 pts) NaOCH3 CH3OH SN2 Br CH3OH SN1 Br NaOCH3 CH3OH E2 Show Zaitsev product Br CH3OH Br E1
1) Name the following molecule: 2) Draw the organic products formed in the following reactions. K.C.07...
1) Name the following molecule: 2) Draw the organic products formed in the following reactions. K.C.07 H₂SO4, H₂o 3) Rank the following organic acids according to strength with 1 being the strongest acid 41 Draw il resonance structures of the fold r Carboxylic acids often exist as dimers, where two molecules are attached to each other Propose a reason. b. Draw an example of this phenomenon between two molecules of acetic acid (CH.COOH) Answer the following questions about the amino...
Predict the major organic product or products of each of the following reactions: Identify the mechanism...
Predict the major organic product or products of each of the
following reactions:
Identify the mechanism taking place in each of the
reactions and please provide explanation.
1. 03 2. Zn/H2O CH,C=CCH, H2 Lindlar's catalyst CH,C=CCH, Li NH3, liquid O3 Zn H2O
Question 4 (10 points) Draw mechanism for the following reactions: -OH a) HO_ Ht 1. Mel b) 2. H'/...
Question 4 (10 points) Draw mechanism for the following reactions: -OH a) HO_ Ht 1. Mel b) 2. H'/H20 Qestion 5 (6 points) Propose a synthesis for the target compound with given starting materials. You may use additional reagents you need. The proposed synthesis should be no more than S steps. Hint: Enolate Reaction, Decarboxylation Reaction. Target Compound Starting Materials
Question 4 (10 points) Draw mechanism for the following reactions: -OH a) HO_ Ht 1. Mel b) 2. H'/H20
Qestion...
1. Predict the major product for the following electrophilic addition reactions. Show the mechanism for each...
1. Predict the major product for the following electrophilic addition reactions. Show the mechanism for each reaction. a. catalytic H2SO4 OH b catalytic H2SO4 H2O catalytic H2SO4 но
3. Predict the major product for each of the following reactions. Show the mechanism and indicate...
3. Predict the major product for each of the following reactions. Show the mechanism and indicate stereochemistry where appropriate. Br Br
3. Predict the major product for each of the following reactions. Show the mechanism and indicate...
3. Predict the major product for each of the following reactions. Show the mechanism and indicate stereochemistry where appropriate. Br Br
3. Predict the major product for each of the following reactions. Show the mechanism and indicate...
3. Predict the major product for each of the following reactions. Show the mechanism and indicate stereochemistry where appropriate. Br-B
Pericyclic Reactions 1. Predict the products of the following reactions and propose a mechanism that explains it Me a heat OMCN heat 9. Ome =-COME HOY Y hest MeOC 2. Propose a synthesis of the following molecules using acetaldehyde as your only starting material 3. Propose a mechanism for the following transformations Meo,
For each of the following reactions, determine which ELIMINATION mechanism (E1 or 2) will occur. Alkyl Halide Substitution: Base Strength: Mechanism Type: 2° 3° Methyl Strong E1 1° Weak E2 Draw the mechanism that leads to ALL products for the reaction. Finally, underline the major product of the elimination reaction: NaOCH Challenge Problems: Synthesis: Predicted Ability: Good Average Poor Actual Ability: Good Average Poor Propose a synthesis from the starting material to obtain the indicated goal molecule. Note that any...
5. Predict the major organic products of the following reactions. Show all asymmetric carbons with wedgeldash notation (i.e., as shown in the starting material). If a reaction produces a racemic mixture, show only one of the enantiomers produced. Carefully note the requested reaction mechanism for each reaction. (20 pts) NaOCH3 CH3OH SN2 Br CH3OH SN1 Br NaOCH3 CH3OH E2 Show Zaitsev product Br CH3OH Br E1
1) Name the following molecule: 2) Draw the organic products formed in the following reactions. K.C.07 H₂SO4, H₂o 3) Rank the following organic acids according to strength with 1 being the strongest acid 41 Draw il resonance structures of the fold r Carboxylic acids often exist as dimers, where two molecules are attached to each other Propose a reason. b. Draw an example of this phenomenon between two molecules of acetic acid (CH.COOH) Answer the following questions about the amino...
Predict the major organic product or products of each of the
following reactions:
Identify the mechanism taking place in each of the
reactions and please provide explanation.
1. 03 2. Zn/H2O CH,C=CCH, H2 Lindlar's catalyst CH,C=CCH, Li NH3, liquid O3 Zn H2O
Question 4 (10 points) Draw mechanism for the following reactions: -OH a) HO_ Ht 1. Mel b) 2. H'/H20 Qestion 5 (6 points) Propose a synthesis for the target compound with given starting materials. You may use additional reagents you need. The proposed synthesis should be no more than S steps. Hint: Enolate Reaction, Decarboxylation Reaction. Target Compound Starting Materials
Question 4 (10 points) Draw mechanism for the following reactions: -OH a) HO_ Ht 1. Mel b) 2. H'/H20
Qestion...
1. Predict the major product for the following electrophilic addition reactions. Show the mechanism for each reaction. a. catalytic H2SO4 OH b catalytic H2SO4 H2O catalytic H2SO4 но
3. Predict the major product for each of the following reactions. Show the mechanism and indicate stereochemistry where appropriate. Br Br
3. Predict the major product for each of the following reactions. Show the mechanism and indicate stereochemistry where appropriate. Br Br
3. Predict the major product for each of the following reactions. Show the mechanism and indicate stereochemistry where appropriate. Br-B
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