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How many hydrogens will a 10-carbon alkene (one double bond, no heteroatoms) have (i.e., C10H22) 16)...
need help with 14-21 Stereochemistry of the Su2 reaction In the Sn2 reaction the tetrahedral carbon...
need help with 14-21
Stereochemistry of the Su2 reaction In the Sn2 reaction the tetrahedral carbon center is inverted. We describe the mechanism as nudeophilic (Nuc) back side attack; the leaving group (LG) is leav ing from the front side. Generally, the LG and the Nucare electron rich so it would be unfavorable for them to react from the same side (charge repuls ion). The geometry of the carbon at the transition state is trigonal planar. 14) Label the 2-bromobuta...
one of the Kekulé structures is not consistent with valence rules? 3. How many degrees of...
one of the Kekulé structures is not consistent with valence rules? 3. How many degrees of unsaturation (double bond equivalents) ore fouand in 3 O-H 4. The regiochemistry of Markovnikov with no rearrangements of alkenes is c. subject to solvent effects 5. The kinetics of this reaction is. a. first-order b. c, cannot be determined 6. Hydroboration/oxidation of alkenes occurs with a. syn b. trans c. anti d. random 7. The reaction of an alkene with dichlorocarbene is: 8. The...
13. How many hydrogens do the following compound have? C9H?NO, has one ring and three double...
13. How many hydrogens do the following compound have? C9H?NO, has one ring and three double bond a. 13 b. 16 c. 12 d. 11
Chapter 11: 1. What is a prime rule in naming alkenes? a. Find the longest carbon...
Chapter 11: 1. What is a prime rule in naming alkenes? a. Find the longest carbon chain. b.Find the longest carbon chain containing the alkene. c. Find whether the alkene has a cis- or trans- configuration. d.Find how far the alkene functionality is from either end. 2. What is the IUPAC name of the following alkene? a. cis-5-methyl-2-heptene b. trans-2-ethyl-4-hexene c. trans-5-methyl-2-heptene d. trans-3-methyl-5-heptene 3. What is the hybridization, geometry, and bond angle of the carbon marked by an asterisk?...
1) What is Zaitsev's rule? (Full answer please.., don't shortcut it.) 2) How many distinct alkenoucts...
1) What is Zaitsev's rule? (Full answer please.., don't shortcut it.) 2) How many distinct alkenoucts an.ossible when the alkyl lodide below undergoes E2 elimination? CH CHs t CH A) 1 B) 2 C) 3 D) 4 E) 5 3) Provide the majer organic product of the reaction below. кон, H2O 4) Provide the structure of the majer organic product in the following reaction. NaOCH3 Ph Ph CH3OH Br 5) Provide the structure of the major alkene product of the...
1) Consider the free radical monochlorination of 3-methylpentane and answer the following: a) How many products...
1) Consider the free radical monochlorination of 3-methylpentane and answer the following: a) How many products (including stereoisomers) are formed? _______ b) How many are chiral? ________ c) Would the major product of free radical bromination possess a chiral carbon? Yes or No 2) Which of the following functional groups can be generated in one step via SN2 or SN1 reaction? (Enter all that apply) a) Aldehyde b) Alcohol c) Alkene d) Alkyne e) Amine f) Carboxylic Acid g) Ester...
need help with 1-21 1) Label the steps below as "slow" and "fast". HCH 013 10...
need help with 1-21
1) Label the steps below as "slow" and "fast". HCH 013 10 = H. C + + H-LG H-LG 2) Why are they slow/fast? Explain using chemical terms. Stereochemistry of the Sn1 reaction 3) What type of intermediate does the Sn1 reaction proceed through? 4) What is the geometry of the carbon that the nucleophile coordinates to in the 2 step? 5) From how many directions would it be reasonable for the nucleophile to approach the...
For letters h & i : For each of the following reactions, predict the major mechanistic pathway (SN1/SN2/E1/E2...
For
letters h & i :
For each of the following reactions, predict the major
mechanistic pathway (SN1/SN2/E1/E2) and the major organic
products
1. (cont.) (h) НСОН CHB -CHBr HCOH - (0) CH,CH,CH,CH,Br- NH 2. For each of the following indicate which reaction will occur faster. Explain your reasoning. (No credit will be given for guesses) (a) The reaction of (CH),CBr with 0.001M aqueous NaOH or 0.10M aqueous NaOH (b) The reaction of 2-bromobutane with NaOH in DMSO or NaSH...
1. (18 points; 3 points each] Multiple Choice: Circle the best answer i. Consider the following...
1. (18 points; 3 points each] Multiple Choice: Circle the best answer i. Consider the following reaction: Xooot THF, A If there are no other changes, what is the effect of doubling the concentration of the starting alcohol on the rate of this reaction? a. No change b. Doubles the rate C. Triples the rate d. Quadruples the rate ii. Which nitrogen compound below would react fastest as a nucleophile in an 5, 2 reaction? NH NH N d. "NH2...
Help on 16, 17, and 18!!!! ? 16. How many constitutional isomer allylic bromides does the...
Help on 16, 17, and 18!!!!
? 16. How many constitutional isomer allylic bromides does the following reaction give? NBS A/hv/ROOR C. 5 a. 3 b.4 d. 6 e. not a.-d. 17. Ignoring stereochemistry, what is the overall enthalpy difference of the reaction of 3-ethylpentane, fluorine, and light going to the major mono-fluorinated product? Bond Disassociation Energies kcal/mole C-H C-F C-CI C-Br C- L X -X 98 107 81 68 53 F | 38 95 106 80 68 53 cl...
need help with 14-21
Stereochemistry of the Su2 reaction In the Sn2 reaction the tetrahedral carbon center is inverted. We describe the mechanism as nudeophilic (Nuc) back side attack; the leaving group (LG) is leav ing from the front side. Generally, the LG and the Nucare electron rich so it would be unfavorable for them to react from the same side (charge repuls ion). The geometry of the carbon at the transition state is trigonal planar. 14) Label the 2-bromobuta...
one of the Kekulé structures is not consistent with valence rules? 3. How many degrees of unsaturation (double bond equivalents) ore fouand in 3 O-H 4. The regiochemistry of Markovnikov with no rearrangements of alkenes is c. subject to solvent effects 5. The kinetics of this reaction is. a. first-order b. c, cannot be determined 6. Hydroboration/oxidation of alkenes occurs with a. syn b. trans c. anti d. random 7. The reaction of an alkene with dichlorocarbene is: 8. The...
13. How many hydrogens do the following compound have? C9H?NO, has one ring and three double bond a. 13 b. 16 c. 12 d. 11
1) What is Zaitsev's rule? (Full answer please.., don't shortcut it.) 2) How many distinct alkenoucts an.ossible when the alkyl lodide below undergoes E2 elimination? CH CHs t CH A) 1 B) 2 C) 3 D) 4 E) 5 3) Provide the majer organic product of the reaction below. кон, H2O 4) Provide the structure of the majer organic product in the following reaction. NaOCH3 Ph Ph CH3OH Br 5) Provide the structure of the major alkene product of the...
need help with 1-21
1) Label the steps below as "slow" and "fast". HCH 013 10 = H. C + + H-LG H-LG 2) Why are they slow/fast? Explain using chemical terms. Stereochemistry of the Sn1 reaction 3) What type of intermediate does the Sn1 reaction proceed through? 4) What is the geometry of the carbon that the nucleophile coordinates to in the 2 step? 5) From how many directions would it be reasonable for the nucleophile to approach the...
For
letters h & i :
For each of the following reactions, predict the major
mechanistic pathway (SN1/SN2/E1/E2) and the major organic
products
1. (cont.) (h) НСОН CHB -CHBr HCOH - (0) CH,CH,CH,CH,Br- NH 2. For each of the following indicate which reaction will occur faster. Explain your reasoning. (No credit will be given for guesses) (a) The reaction of (CH),CBr with 0.001M aqueous NaOH or 0.10M aqueous NaOH (b) The reaction of 2-bromobutane with NaOH in DMSO or NaSH...
1. (18 points; 3 points each] Multiple Choice: Circle the best answer i. Consider the following reaction: Xooot THF, A If there are no other changes, what is the effect of doubling the concentration of the starting alcohol on the rate of this reaction? a. No change b. Doubles the rate C. Triples the rate d. Quadruples the rate ii. Which nitrogen compound below would react fastest as a nucleophile in an 5, 2 reaction? NH NH N d. "NH2...
Help on 16, 17, and 18!!!!
? 16. How many constitutional isomer allylic bromides does the following reaction give? NBS A/hv/ROOR C. 5 a. 3 b.4 d. 6 e. not a.-d. 17. Ignoring stereochemistry, what is the overall enthalpy difference of the reaction of 3-ethylpentane, fluorine, and light going to the major mono-fluorinated product? Bond Disassociation Energies kcal/mole C-H C-F C-CI C-Br C- L X -X 98 107 81 68 53 F | 38 95 106 80 68 53 cl...
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