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can you please solve everything
9 Give an example of a synthesis that requires the protection...
can you solve everything please Short Answer 7. Show how you could synthesize these compounds from...
can you solve everything please
Short Answer 7. Show how you could synthesize these compounds from any compound having three carbons or fewer. You can use any regent necessary, but keep to the three carbons. Сн, снен, с-н снен, сн, ск, сн, сн, 8. Give an example of a synthesis that requires the protection of an ketone. You may use any reaction, any organic compounds. You must show the reaction that does the protecting. 9. Give an example of a...
can many re c essary, but keep to the three care Сн, снен, с-н сненсн, снен,...
can many re c essary, but keep to the three care Сн, снен, с-н сненсн, снен, сн. 8. Give an example of a synthesis that requires the protection of an ketone. You may use any reaction, any organic compounds. You must show the reaction that does the protecting.
3) Devise a synthesis of the following compound using the given compounds (you may use each...
3) Devise a synthesis of the following compound using the given compounds (you may use each one more than once if needed). You may also use any needed inorganic or organic reagents but all of the carbons in the target molecule must come from the given starting materials. Hint: this synthesis will require you to use ozonolysis and a reaction that starts with the letter DI
IM HAVING DIFFICULTIES TO IDENTIFY NMR, can you please explain in details this answer and whats t...
IM HAVING DIFFICULTIES TO IDENTIFY NMR, can you please explain
in details this answer and whats the easiest way to read it
The reaction is worked up and compared to the starting material by NMR Staring material (methyl (S 2-methy-4-cxobutanoate) Product зн 러 зн H 24 3H 2H 10 PPM 2 PPM Question #14: Does it appear that the correct product has formed? Examine your reasoning type your text here For example, if you had an alcohol and an aldehyde...
extra credit orgo chem NaBH MOH 1.Write two starting materials (five or fewer C's) that react...
extra credit orgo chem
NaBH MOH 1.Write two starting materials (five or fewer C's) that react to form the target molecule starting from any carbonyl compound and any organometallic reagent. OH Part IV. Mechanistic Puzzlers (16 pts) 10. Reduction of cyclohexanone using lithium aluminum hydride gives a deuterated alcohol when D.O is used instead of H.O in the workup step. Account for this outcome with a mechanism, showing curved arrows, the key intermediate, and lone pairs and charges. (6 pts)...
can you please answer both questions Devise a synthesis of these compounds starting with three-carbon alkyl...
can you please answer both questions
Devise a synthesis of these compounds starting with three-carbon alkyl halides. Show any necessary reagents and reaction conditions. All carbons must ultimately come from the 3-carbon alkyl halides. Once you have made a new compound you may reuse it without making it again. Butanone Br -OH OH PCL Butanoic acid or CEN N ENHOS Dr structures of t 0.8 h e CHO 0.6 0.41 3000 1000 2000 Wavenumber (cm-1) CHO ETHER 0:11 No D.u...
Can someone help me to solve this problem. Please good handwritting and with explain everything thank...
Can someone help me to solve this problem.
Please
good handwritting and with explain
everything
thank you
1. (12 pts) Reaction Prediction. For each reaction below: o Write a balanced equation or write "no reaction" * Specify the phase of each compound. Identify the type of reaction a) octane, CeHi8 burns in oxygen b) reaction of nitric acid with sodium hydroxide2 c) CuCl2 (aq) reacted with K2S04 (ag) Zs) (aay) d) HCIO3 added to CaCOs td) e) a solution of...
can you solve everything Instructions: Consider the reaction below to answer the following question. На но...
can you solve everything
Instructions: Consider the reaction below to answer the following question. На но носH,сH,он в 4. Refer to instructions. The electrophile, the nucleophile and the catalyst in this reaction are indicated by letters respectively and Multiple Choice Identify the choice that best completes the statement or answers the question S. Many nucleophilic addition reactions of aldehydes and ketones are catalyzed by acid or base. Bases catalyze hydration by: a. converting the water to hydroxide ion, a much...
9.RETROSYNTHETIC ANALYSIS Give a reasonable synthesis for the following compound from the indicated starting materials. You...
9.RETROSYNTHETIC ANALYSIS Give a reasonable synthesis for the following compound from the indicated starting materials. You may use any other organic reagents or inorganic reagents you wish. The desired product for each reaction must be the MAJOR PRODUCT. Give the reactants, conditions (where appropriate), and products of each synthetic step but NO MECHANISMS. [4 points) OH Use to make HO
can questions 1-9 please be answered and why are they the answer 1. How many sp...
can questions 1-9 please be answered and why are they the
answer
1. How many sp hybridized carbon atoms are present in the following molecule? (A) 3 (B) 4 5 н.с (D). 6 2. Which bond is the longest in the following molecule? (A) (B) CECH (C) (D) 3. Which of the following molecules is chiral at room tempernture (25 C)? (A) 1,1-dimethylcyclohexane (B) cis-1,2-dimethyleyelohexanc (C) trans-,3-dimethyleyclohexane (D) trans-1,4-dimethylcyclohexane 4. Which group is an aldehyde? н н (C) (D) (A)...
can you solve everything please
Short Answer 7. Show how you could synthesize these compounds from any compound having three carbons or fewer. You can use any regent necessary, but keep to the three carbons. Сн, снен, с-н снен, сн, ск, сн, сн, 8. Give an example of a synthesis that requires the protection of an ketone. You may use any reaction, any organic compounds. You must show the reaction that does the protecting. 9. Give an example of a...
can many re c essary, but keep to the three care Сн, снен, с-н сненсн, снен, сн. 8. Give an example of a synthesis that requires the protection of an ketone. You may use any reaction, any organic compounds. You must show the reaction that does the protecting.
3) Devise a synthesis of the following compound using the given compounds (you may use each one more than once if needed). You may also use any needed inorganic or organic reagents but all of the carbons in the target molecule must come from the given starting materials. Hint: this synthesis will require you to use ozonolysis and a reaction that starts with the letter DI
IM HAVING DIFFICULTIES TO IDENTIFY NMR, can you please explain
in details this answer and whats the easiest way to read it
The reaction is worked up and compared to the starting material by NMR Staring material (methyl (S 2-methy-4-cxobutanoate) Product зн 러 зн H 24 3H 2H 10 PPM 2 PPM Question #14: Does it appear that the correct product has formed? Examine your reasoning type your text here For example, if you had an alcohol and an aldehyde...
extra credit orgo chem
NaBH MOH 1.Write two starting materials (five or fewer C's) that react to form the target molecule starting from any carbonyl compound and any organometallic reagent. OH Part IV. Mechanistic Puzzlers (16 pts) 10. Reduction of cyclohexanone using lithium aluminum hydride gives a deuterated alcohol when D.O is used instead of H.O in the workup step. Account for this outcome with a mechanism, showing curved arrows, the key intermediate, and lone pairs and charges. (6 pts)...
can you please answer both questions
Devise a synthesis of these compounds starting with three-carbon alkyl halides. Show any necessary reagents and reaction conditions. All carbons must ultimately come from the 3-carbon alkyl halides. Once you have made a new compound you may reuse it without making it again. Butanone Br -OH OH PCL Butanoic acid or CEN N ENHOS Dr structures of t 0.8 h e CHO 0.6 0.41 3000 1000 2000 Wavenumber (cm-1) CHO ETHER 0:11 No D.u...
Can someone help me to solve this problem.
Please
good handwritting and with explain
everything
thank you
1. (12 pts) Reaction Prediction. For each reaction below: o Write a balanced equation or write "no reaction" * Specify the phase of each compound. Identify the type of reaction a) octane, CeHi8 burns in oxygen b) reaction of nitric acid with sodium hydroxide2 c) CuCl2 (aq) reacted with K2S04 (ag) Zs) (aay) d) HCIO3 added to CaCOs td) e) a solution of...
can you solve everything
Instructions: Consider the reaction below to answer the following question. На но носH,сH,он в 4. Refer to instructions. The electrophile, the nucleophile and the catalyst in this reaction are indicated by letters respectively and Multiple Choice Identify the choice that best completes the statement or answers the question S. Many nucleophilic addition reactions of aldehydes and ketones are catalyzed by acid or base. Bases catalyze hydration by: a. converting the water to hydroxide ion, a much...
9.RETROSYNTHETIC ANALYSIS Give a reasonable synthesis for the following compound from the indicated starting materials. You may use any other organic reagents or inorganic reagents you wish. The desired product for each reaction must be the MAJOR PRODUCT. Give the reactants, conditions (where appropriate), and products of each synthetic step but NO MECHANISMS. [4 points) OH Use to make HO
can questions 1-9 please be answered and why are they the
answer
1. How many sp hybridized carbon atoms are present in the following molecule? (A) 3 (B) 4 5 н.с (D). 6 2. Which bond is the longest in the following molecule? (A) (B) CECH (C) (D) 3. Which of the following molecules is chiral at room tempernture (25 C)? (A) 1,1-dimethylcyclohexane (B) cis-1,2-dimethyleyelohexanc (C) trans-,3-dimethyleyclohexane (D) trans-1,4-dimethylcyclohexane 4. Which group is an aldehyde? н н (C) (D) (A)...
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