please help explain how I figure this out
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please help explain how I figure this out
Br 23. Which of these structures best depicts...
Please help! I need to name these structures but I can't figure them out (the most...
Please help! I need to name these structures but I can't figure
them out (the most important ones are 15 and 16).
# Compound Structure 1 H Η Η Η ΤΙΤΙ H-C-C-C-C-H ΤΙ Η Η Η Η H 2 H-C=C-C-H ει-- Η H 3 HEC-H Η H Η 4 C- H H 5 Η Η Η Η H ΤΙΤΙ H,C-C-C-C-C-C=C-C-H ΤΙΤΙ Η Η Η Η Η T H 6 Η Η Η TTI C=C-C-C-CH3 ΤΙ Η Η 7 Η Η...
please help in all questions!! Which of the molecules below is the expected major product of...
please help in all questions!!
Which of the molecules below is the expected major product of the following reduction? Na, NH3) Н H Н нн H H For the given compounds answer the following. Compound A Compound B Compound C Identify which compound is expected to be most acidic. Compound A Compound B Compound C Choose the correct option to justify your choice. ODeprotonation of the compound generates an antiaromatic lon. Deprotonation of the compound generates an aromatic ion. Deprotonation...
Organic Chemistry please help asap 70. What nucleophiles wou cleophiles would form the following compounds as...
Organic Chemistry please help asap
70. What nucleophiles wou cleophiles would form the following compounds as a result of reacting with l-iodobutane? OH SH 11. Draw (R)-2-bromopentane + CHO b. (R)-3-bromo-3-methylheptane + CH,OH c. benzyl chloride + CH CH OH te tollowing reactions: if the products can exist as stereoisomers, show what striscmers are obtained d. allyl chloride + CHOH e. 1-bromo-2-butene + CHO 1. l-bromo-2-butene + CH OH the products obtained from the solvolysis of each of the following...
I need help on all of these please 1. Draw the energy diagram that correctly depicts...
I need help on all of these please
1. Draw the energy diagram that correctly depicts the following reaction (AG<0) and the transition state for the rate determining step. Label substrate (S), product (P), and intermediate (1) if applicable. OTS + NaBr TsONa polar aprotic solvent transition state free energy reaction progress 2. Complete the following reaction schemes. CH3OH 0°C alkyl halide nucleophile ТА polar aprotic solvent 3. Compound A and B are constitutional isomers with molecular formula C5H11Br. When...
please help! 1) Which of the following compounds is chiral? CH3-1-ci CH3-1-ci Br -1-ci CH3 CH3-1-Br...
please help!
1) Which of the following compounds is chiral? CH3-1-ci CH3-1-ci Br -1-ci CH3 CH3-1-Br CH3-1-ci CH3 3-1-C CH3 CH3 ci--c1 Br--Br CH3 2) What is the relationship between the structures shown below? H-|-Brand Br- -CH3 CH3 o Constitutional isomers Identical compounds O Diastereomers O Enantiomers O Configurational isomers 4) What is the product of the following reaction? MoBr 2. Fich, o V. HOCHẶCHỌCH-O V. II. CH CHCH-(O) OH CH2OH ON CH3CH II. HOCH2CH2– O III oll ON 01...
Which set of reaction conditions represents the best way to carry out the following transformation? Briefly...
Which set of reaction conditions represents the best way to
carry out the following transformation? Briefly explain your choice
using one sentence.
T I 1111 CH ... CH3 H OCOCH Br OCOCH a) CH3COOCH2CH3 in water b) CH3COONa in DMSO c) CH3COONa in water d) CH3COONa in acetone
draw out structures or reagents Draw out either the structures or the reagents A-Q needed to...
draw out structures or reagents
Draw out either the structures or the reagents A-Q needed to complete the reaction roadmap below 1) CuLi(CH-CH(), 0 2) H.O 1) Mg 2) formaldehyde Br 3) H30 G H2C1 CH3 HyC N B 1)Bry(excess), NaOH 2)HCI PCC F PBr3 E NaOH A Р I 1) Dibal 2) H,O, CH Nz, ether HCI 1) TOSCI, pyridine 2) NaH SOCI J 1) NaBr 2) H30 H M 1) 2CH,MgBr 2) H,O, HCI HECHC=CH2 Acetic Acid NaOCH...
can someone please explain how to do this with as much detail as possible. someone tried...
can someone please explain how to do this with as much detail
as possible. someone tried to explain it earlier in relation to
(a,e) and (e,a) but im not sure even what that means
Bccurance of Methyl shift o. The following two elimination reactions are found to have very different rates of reaction. The cis compound produces two products and it reacts much faster than the trans isomer, which produces only one product. Explain these observations (the erence in rate...
help with all please 14. Which of the following mechanistically depicts the protonation of tert-butyl alcohol...
help with all please
14. Which of the following mechanistically depicts the protonation of tert-butyl alcohol by hydrogen bromide? H-Br: в) (CH);С —ӧ: A) (CH3)3C-ö: н- Br: Н H-Br н D) (CH3)3C-ö H- Вr: C) (CH3)3CÖ: d. D c. C b.B a. A 15. What would by the effect of doubling both the concentration of t-butyl bromide and the concentration of sodium iodide in the reaction of t-butyl bromide with sodium iodide in methanol? a. The rate stays the same....
Which option (A,B,C, or D) is the best way to synthesize the ether shown? Figure 8.8...
Which option (A,B,C, or D) is the best way to synthesize the ether
shown?
Figure 8.8 x or A. X Br + o CH₂ CH3 - B. X or + Br Chtechts - c. X oH + - o Ctzeltz - D. t Br+ Br CH₂ CH3 →
Please help! I need to name these structures but I can't figure
them out (the most important ones are 15 and 16).
# Compound Structure 1 H Η Η Η ΤΙΤΙ H-C-C-C-C-H ΤΙ Η Η Η Η H 2 H-C=C-C-H ει-- Η H 3 HEC-H Η H Η 4 C- H H 5 Η Η Η Η H ΤΙΤΙ H,C-C-C-C-C-C=C-C-H ΤΙΤΙ Η Η Η Η Η T H 6 Η Η Η TTI C=C-C-C-CH3 ΤΙ Η Η 7 Η Η...
please help in all questions!!
Which of the molecules below is the expected major product of the following reduction? Na, NH3) Н H Н нн H H For the given compounds answer the following. Compound A Compound B Compound C Identify which compound is expected to be most acidic. Compound A Compound B Compound C Choose the correct option to justify your choice. ODeprotonation of the compound generates an antiaromatic lon. Deprotonation of the compound generates an aromatic ion. Deprotonation...
Organic Chemistry please help asap
70. What nucleophiles wou cleophiles would form the following compounds as a result of reacting with l-iodobutane? OH SH 11. Draw (R)-2-bromopentane + CHO b. (R)-3-bromo-3-methylheptane + CH,OH c. benzyl chloride + CH CH OH te tollowing reactions: if the products can exist as stereoisomers, show what striscmers are obtained d. allyl chloride + CHOH e. 1-bromo-2-butene + CHO 1. l-bromo-2-butene + CH OH the products obtained from the solvolysis of each of the following...
I need help on all of these please
1. Draw the energy diagram that correctly depicts the following reaction (AG<0) and the transition state for the rate determining step. Label substrate (S), product (P), and intermediate (1) if applicable. OTS + NaBr TsONa polar aprotic solvent transition state free energy reaction progress 2. Complete the following reaction schemes. CH3OH 0°C alkyl halide nucleophile ТА polar aprotic solvent 3. Compound A and B are constitutional isomers with molecular formula C5H11Br. When...
please help!
1) Which of the following compounds is chiral? CH3-1-ci CH3-1-ci Br -1-ci CH3 CH3-1-Br CH3-1-ci CH3 3-1-C CH3 CH3 ci--c1 Br--Br CH3 2) What is the relationship between the structures shown below? H-|-Brand Br- -CH3 CH3 o Constitutional isomers Identical compounds O Diastereomers O Enantiomers O Configurational isomers 4) What is the product of the following reaction? MoBr 2. Fich, o V. HOCHẶCHỌCH-O V. II. CH CHCH-(O) OH CH2OH ON CH3CH II. HOCH2CH2– O III oll ON 01...
Which set of reaction conditions represents the best way to
carry out the following transformation? Briefly explain your choice
using one sentence.
T I 1111 CH ... CH3 H OCOCH Br OCOCH a) CH3COOCH2CH3 in water b) CH3COONa in DMSO c) CH3COONa in water d) CH3COONa in acetone
draw out structures or reagents
Draw out either the structures or the reagents A-Q needed to complete the reaction roadmap below 1) CuLi(CH-CH(), 0 2) H.O 1) Mg 2) formaldehyde Br 3) H30 G H2C1 CH3 HyC N B 1)Bry(excess), NaOH 2)HCI PCC F PBr3 E NaOH A Р I 1) Dibal 2) H,O, CH Nz, ether HCI 1) TOSCI, pyridine 2) NaH SOCI J 1) NaBr 2) H30 H M 1) 2CH,MgBr 2) H,O, HCI HECHC=CH2 Acetic Acid NaOCH...
can someone please explain how to do this with as much detail
as possible. someone tried to explain it earlier in relation to
(a,e) and (e,a) but im not sure even what that means
Bccurance of Methyl shift o. The following two elimination reactions are found to have very different rates of reaction. The cis compound produces two products and it reacts much faster than the trans isomer, which produces only one product. Explain these observations (the erence in rate...
help with all please
14. Which of the following mechanistically depicts the protonation of tert-butyl alcohol by hydrogen bromide? H-Br: в) (CH);С —ӧ: A) (CH3)3C-ö: н- Br: Н H-Br н D) (CH3)3C-ö H- Вr: C) (CH3)3CÖ: d. D c. C b.B a. A 15. What would by the effect of doubling both the concentration of t-butyl bromide and the concentration of sodium iodide in the reaction of t-butyl bromide with sodium iodide in methanol? a. The rate stays the same....
Which option (A,B,C, or D) is the best way to synthesize the ether
shown?
Figure 8.8 x or A. X Br + o CH₂ CH3 - B. X or + Br Chtechts - c. X oH + - o Ctzeltz - D. t Br+ Br CH₂ CH3 →
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