please explain fully thanksHomework Answers
based on the type of alkyl halide and the solvents the
possible reactants and the reagent conditions are as
follows
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please explain fully thanks
12. Each of the following compounds can be prepared with an alkyl...
OH The compand can be prepared with on alkyl iodide & a suitable nucleophile. Identify the...
OH The compand can be prepared with on alkyl iodide & a suitable nucleophile. Identify the alkyl iodide & nucleophile that you would use. For onionic nucleophile you don't need to draw Counterion,
(12 points) Esters can be prepared by nucleophilic substitution of an alkyl halide or via acyl su...
(12 points) Esters can be prepared by nucleophilic substitution of an alkyl halide or via acyl substitution reactions. Show the compounds required to synthesize the ester two different ways. Be sure the product will be favored. 4. H0 alkyl halide nucleophile acyl derivative nucleophile Given the information in the question above, provide appropriate reactants above. hat does a nucleophilic substitution reaction look like in general? Acyl substitution?
(12 points) Esters can be prepared by nucleophilic substitution of an alkyl halide...
Can you please explain how to solve only 7.62 and 7.64? As well as 6.28 a...
Can you please explain how to solve only 7.62 and 7.64? As well
as 6.28 a and b.
Rank the three carbocations shown in terms of increasing stability: 6.28 (a) nobicnensh (b) owllo or 3 DE 7.62 Predict the stereochemical outcome for each of the following E reactions. In each case, draw only the major product of the reaction (a) ? NaOH (b) CN Br (a) (c) ? NaOH in the substrate. in the product. CI (b) (d) of configuration?...
Please help and explain each Thanks. In which of the following compounds does the bond between...
Please help and explain each
Thanks.
In which of the following compounds does the bond between the central atom and fluorine have the highest percent ionic character? Select one: a. AsF3 b. SeF2 c. OF2 d. SbF3 e. SF2
can someone please explain this to me? Which of the following compounds were synthesized via an...
can someone please explain this to me?
Which of the following compounds were synthesized via an ALDOL reaction?! Use the picture below to choose your answer(s) он о он он ОН о Ph он
Answer Questions 3 & 4 please Rank each of the following sets of compounds in order...
Answer Questions 3 & 4 please
Rank each of the following sets of compounds in order of increase acidity A (a) CH4 (b) CHCI; (c) CH3CI (d) CH2Cl2 CI B (a) OH (b) (c) OH ОН (а) (b) OH 4. Complete the following reactions (use curved arrows to show the flow of electron pairs in each reaction) and label the reagent that acts as a nucleophile and the one that acts as electrophile. If any. A CH3CO2H + OH- B...
Can you please draw it and explain Which of the following compounds is the product of...
Can you please draw it and explain
Which of the following compounds is the product of the reaction shown that displays retention of configuration compared to the starting material? H2O Sni a . H d. HO, b. Br CH3 H H3C он OH c. CH3
3) Which of the following acids can be prepared by a malonic ester synthesis? Show th...
3) Which of the following acids can be prepared by a malonic ester synthesis? Show th steps and the reagents you would use. соон b) a) COOH c) COOH d) 4) The following compounds can be made using the aldol condensation. Write the steps and reagents you would use. -CHO b) a) CHO c) он d) он о
please explain fully with details. thanks 6. Predict the major product(s) for each of the following...
please explain fully with details. thanks
6. Predict the major product(s) for each of the following reactions. Include Swi regiochemistry/stereochemistry where appropriate. HCI b) ? Brą, H20 1) Hg(OAC)2, H20 2) NaBH4 1) BH3, THE 2) H2O2, NaOH e) ? 1) MCPBA 3) 2 , Hyor 1) O3 2) Zn, H30*
Show how each of the following compounds could be prepared using the given starting materials. Please...
Show how each of the following compounds could be prepared using
the given starting materials. Please Explain
#Show how each of the following compounds could be prepared using the given starting materials, @ HCECH → M © HECH -Y © HC ECH - > D = sehr HCECH (35,4R)-4-bromo-3-hexanol and (30,45) -4- bromo-3-hexand
OH The compand can be prepared with on alkyl iodide & a suitable nucleophile. Identify the alkyl iodide & nucleophile that you would use. For onionic nucleophile you don't need to draw Counterion,
(12 points) Esters can be prepared by nucleophilic substitution of an alkyl halide or via acyl substitution reactions. Show the compounds required to synthesize the ester two different ways. Be sure the product will be favored. 4. H0 alkyl halide nucleophile acyl derivative nucleophile Given the information in the question above, provide appropriate reactants above. hat does a nucleophilic substitution reaction look like in general? Acyl substitution?
(12 points) Esters can be prepared by nucleophilic substitution of an alkyl halide...
Can you please explain how to solve only 7.62 and 7.64? As well
as 6.28 a and b.
Rank the three carbocations shown in terms of increasing stability: 6.28 (a) nobicnensh (b) owllo or 3 DE 7.62 Predict the stereochemical outcome for each of the following E reactions. In each case, draw only the major product of the reaction (a) ? NaOH (b) CN Br (a) (c) ? NaOH in the substrate. in the product. CI (b) (d) of configuration?...
Please help and explain each
Thanks.
In which of the following compounds does the bond between the central atom and fluorine have the highest percent ionic character? Select one: a. AsF3 b. SeF2 c. OF2 d. SbF3 e. SF2
can someone please explain this to me?
Which of the following compounds were synthesized via an ALDOL reaction?! Use the picture below to choose your answer(s) он о он он ОН о Ph он
Answer Questions 3 & 4 please
Rank each of the following sets of compounds in order of increase acidity A (a) CH4 (b) CHCI; (c) CH3CI (d) CH2Cl2 CI B (a) OH (b) (c) OH ОН (а) (b) OH 4. Complete the following reactions (use curved arrows to show the flow of electron pairs in each reaction) and label the reagent that acts as a nucleophile and the one that acts as electrophile. If any. A CH3CO2H + OH- B...
Can you please draw it and explain
Which of the following compounds is the product of the reaction shown that displays retention of configuration compared to the starting material? H2O Sni a . H d. HO, b. Br CH3 H H3C он OH c. CH3
3) Which of the following acids can be prepared by a malonic ester synthesis? Show th steps and the reagents you would use. соон b) a) COOH c) COOH d) 4) The following compounds can be made using the aldol condensation. Write the steps and reagents you would use. -CHO b) a) CHO c) он d) он о
please explain fully with details. thanks
6. Predict the major product(s) for each of the following reactions. Include Swi regiochemistry/stereochemistry where appropriate. HCI b) ? Brą, H20 1) Hg(OAC)2, H20 2) NaBH4 1) BH3, THE 2) H2O2, NaOH e) ? 1) MCPBA 3) 2 , Hyor 1) O3 2) Zn, H30*
Show how each of the following compounds could be prepared using
the given starting materials. Please Explain
#Show how each of the following compounds could be prepared using the given starting materials, @ HCECH → M © HECH -Y © HC ECH - > D = sehr HCECH (35,4R)-4-bromo-3-hexanol and (30,45) -4- bromo-3-hexand
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