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just part D & E please Part I. Provide an analysis (show starting materials) and detailed...
5. (12 pts) For the molecules below, provide a retrosynthetic analysis to starting materials that satisfy...
5. (12 pts) For the molecules below, provide a retrosynthetic analysis to starting materials that satisfy the conditions given. Then give a step-by-step synthetic plan. You may use any reagents you want to accomplish your synthesis. OH O from starting materials containing three or fewer carbon atoms from starting materials containing two or fewer carbon atoms
4. (12 pts) For each of the molecules below, provide a retrosynthetic analysis to starting materials...
4. (12 pts) For each of the molecules below, provide a retrosynthetic analysis to starting materials that satisfy the conditions given. Then give a step-by-step synthetic plan. You may use any reagents you want to accomplish your synthesis. HC НОХ H₃C CH весна from propanal as the only carbon source from starting materials containing three or fewer carbon atoms
please show all steps with necessary mechanism arrows 1. Provide the starting specific nucleophile and electrophile...
please show all steps with necessary mechanism arrows
1. Provide the starting specific nucleophile and electrophile that would result in each of the following molecules using an SN2 reaction. Do consider the ABC and provide the specific reagent necessary. (2 points) Me HH MeMe Me I wyn Me Me 2. Provide a detailed retrosynthesis and synthesis of the following compound from the indicated starting material. All atoms of the target must come from the indicated starting materials. You may use...
Please show your work thanks Snow how to prepare the product shown below, using only ethane as the source of carbon. Yo...
Please show your work thanks
Snow how to prepare the product shown below, using only ethane as the source of carbon. You can reagent that is needed to accomplish the synthesis, but the final carbons in the compound must nav , but the final carbons in the compound must have come from etnane. Use retrosynthesis analysis and the special arrow) to work backwards to the starting material mnen, show the complete sequence using the "regular" reaction arrow. (Note (hint) that...
can someone show me mechanisms please *2 6 points) Provide a reasonable synthesis of each of the molecules shown ang...
can someone show me mechanisms please
*2 6 points) Provide a reasonable synthesis of each of the molecules shown ang from the indicated starting material, and using any organic or inorganic reagents. The synthesis The synthesis may require more than one sten. You must write the reagents in correct sequence. Remember to work backward from the product starting material. No mechanism. Br ???? LOH OH racemic 1) NO DE+E+0H 2) KMnO4 NaOH cold (or 0504) ???? racemic E- Alkene 1)...
PLEASE SHOW ALL WORK AND PLEASE ANSWER ALL PARTS OF EACH QUESTION! Thank you! 06 Question (4 points) e See page 574 Comp...
PLEASE SHOW ALL WORK AND
PLEASE ANSWER ALL PARTS OF EACH QUESTION! Thank you!
06 Question (4 points) e See page 574 Complete the mechanism. All necessary atoms and bonds (that is, those that are involved in the mechanism) are drawn in for you already; do not modify the structures by adding or removing any atoms. 1st attempt See Periodic Table See Hint Add the missing curved arrow notation. e See pa 09 Question (4 points) Predict the organic starting...
13 SN1: Synthesis of tert-Butyl Chloride Alkyl halides can be prepared from their corresponding alcohols via...
13 SN1: Synthesis of tert-Butyl Chloride Alkyl halides can be prepared from their corresponding alcohols via an acid catalyzed substitution reaction. The mechanism of these acid catalyzed substitution reactions are labeled as SNI (substitution, nucleophilic, unimolecular) and S 2 (substitution, nucleophilic, bimolecular). Tertiary alcohols follow the Syl route, primary alcohols follow the Sy2 route, and secondary alcohols can follow either path. Under acidic conditions, the mechanism (Figure 1) of the Syl reaction involves rapid protonation of the alcohol, followed by...
Please help I need any idea of what to do CHE 282- Spring 2018-Labo: Planning Multistep...
Please help I need any idea of what to do
CHE 282- Spring 2018-Labo: Planning Multistep Synthesis of an Organic compound. 18 points Due Week of April 23 before start of Lab 10 (Late assignments penalty- 1 point per hour) Name Partner: TA: You are Student 1 Complete and submit this worksheet Attach more sheets of paper as needed L7.Leonides L7-Leonides Problem 1: Using any technique and chemical reaction(s) covered in CHE 201-202 prepare a proposed synthetic plan to show...
How to solve alkene and alkyne reactions - Merdanym i Act antalyzod Hrdian ca Come Lazarmistry...
How to solve alkene and alkyne reactions
- Merdanym i Act antalyzod Hrdian ca Come Lazarmistry I V WORKSHOP #9 Alkenes, Alkynes, Reactions 1. Give a reasonable mechanism for the following reaction. Clearly show intermediates and show the movement of electron pairs with curved arrows. all сна H20. (H2SO4) H₃C CH₂ нас он H3CX сна 2. The addition of HBr to 2-methylpropene can, in principle, give either 1-bromo-2- methylpropane or 2-bromo-2-methylpropane. In reality, only the latter is formed. Show mechanisms...
1.) (9 points) Give structures for the following compounds: a) meta-phenylphenol b) 6-benzyl-3-heptanol e) ortho-sec-butyltoluene 2.)...
1.) (9 points) Give structures for the following compounds: a) meta-phenylphenol b) 6-benzyl-3-heptanol e) ortho-sec-butyltoluene 2.) (9 points) Name the following compounds: 3.) (8 points) Label the following molecules as aromatic, anti-aromatic, or non-aromatic. For the ones th aren't aromatic, explain why they are either non-aromatic or anti-aromatic. 0.8 4.) (11 points) For the following electrophilic aromatic substitution reaction: Вт, FeBr; a) Which product is the major one? b) Draw a complete mechanism for the formation of the major product...
5. (12 pts) For the molecules below, provide a retrosynthetic analysis to starting materials that satisfy the conditions given. Then give a step-by-step synthetic plan. You may use any reagents you want to accomplish your synthesis. OH O from starting materials containing three or fewer carbon atoms from starting materials containing two or fewer carbon atoms
4. (12 pts) For each of the molecules below, provide a retrosynthetic analysis to starting materials that satisfy the conditions given. Then give a step-by-step synthetic plan. You may use any reagents you want to accomplish your synthesis. HC НОХ H₃C CH весна from propanal as the only carbon source from starting materials containing three or fewer carbon atoms
please show all steps with necessary mechanism arrows
1. Provide the starting specific nucleophile and electrophile that would result in each of the following molecules using an SN2 reaction. Do consider the ABC and provide the specific reagent necessary. (2 points) Me HH MeMe Me I wyn Me Me 2. Provide a detailed retrosynthesis and synthesis of the following compound from the indicated starting material. All atoms of the target must come from the indicated starting materials. You may use...
Please show your work thanks
Snow how to prepare the product shown below, using only ethane as the source of carbon. You can reagent that is needed to accomplish the synthesis, but the final carbons in the compound must nav , but the final carbons in the compound must have come from etnane. Use retrosynthesis analysis and the special arrow) to work backwards to the starting material mnen, show the complete sequence using the "regular" reaction arrow. (Note (hint) that...
can someone show me mechanisms please
*2 6 points) Provide a reasonable synthesis of each of the molecules shown ang from the indicated starting material, and using any organic or inorganic reagents. The synthesis The synthesis may require more than one sten. You must write the reagents in correct sequence. Remember to work backward from the product starting material. No mechanism. Br ???? LOH OH racemic 1) NO DE+E+0H 2) KMnO4 NaOH cold (or 0504) ???? racemic E- Alkene 1)...
PLEASE SHOW ALL WORK AND
PLEASE ANSWER ALL PARTS OF EACH QUESTION! Thank you!
06 Question (4 points) e See page 574 Complete the mechanism. All necessary atoms and bonds (that is, those that are involved in the mechanism) are drawn in for you already; do not modify the structures by adding or removing any atoms. 1st attempt See Periodic Table See Hint Add the missing curved arrow notation. e See pa 09 Question (4 points) Predict the organic starting...
13 SN1: Synthesis of tert-Butyl Chloride Alkyl halides can be prepared from their corresponding alcohols via an acid catalyzed substitution reaction. The mechanism of these acid catalyzed substitution reactions are labeled as SNI (substitution, nucleophilic, unimolecular) and S 2 (substitution, nucleophilic, bimolecular). Tertiary alcohols follow the Syl route, primary alcohols follow the Sy2 route, and secondary alcohols can follow either path. Under acidic conditions, the mechanism (Figure 1) of the Syl reaction involves rapid protonation of the alcohol, followed by...
Please help I need any idea of what to do
CHE 282- Spring 2018-Labo: Planning Multistep Synthesis of an Organic compound. 18 points Due Week of April 23 before start of Lab 10 (Late assignments penalty- 1 point per hour) Name Partner: TA: You are Student 1 Complete and submit this worksheet Attach more sheets of paper as needed L7.Leonides L7-Leonides Problem 1: Using any technique and chemical reaction(s) covered in CHE 201-202 prepare a proposed synthetic plan to show...
How to solve alkene and alkyne reactions
- Merdanym i Act antalyzod Hrdian ca Come Lazarmistry I V WORKSHOP #9 Alkenes, Alkynes, Reactions 1. Give a reasonable mechanism for the following reaction. Clearly show intermediates and show the movement of electron pairs with curved arrows. all сна H20. (H2SO4) H₃C CH₂ нас он H3CX сна 2. The addition of HBr to 2-methylpropene can, in principle, give either 1-bromo-2- methylpropane or 2-bromo-2-methylpropane. In reality, only the latter is formed. Show mechanisms...
1.) (9 points) Give structures for the following compounds: a) meta-phenylphenol b) 6-benzyl-3-heptanol e) ortho-sec-butyltoluene 2.) (9 points) Name the following compounds: 3.) (8 points) Label the following molecules as aromatic, anti-aromatic, or non-aromatic. For the ones th aren't aromatic, explain why they are either non-aromatic or anti-aromatic. 0.8 4.) (11 points) For the following electrophilic aromatic substitution reaction: Вт, FeBr; a) Which product is the major one? b) Draw a complete mechanism for the formation of the major product...
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