9. Write out the mechanism for: MACN > Sw2 10. a) Write out 6 completely different...
Please answer the ENTIRE page. #9-11.
9. Write out the mechanism for CA3 CH3OH SN 10. a) Write out 6 completely different reactions of cyclohexanone (reagent product) b) Write out 3 preparations of 2-butanol, a different starting material for each one. In some preps you just have to change the functional group; in other preps you may have to construct the carbon chain. c) Write out 3 preparations of (CHs),CCH;CH2COH, a different starting material for each one. In some preps...
question 9, 10c and 11 need answers
9. Write out the mechanism for: MSH CH₂ SNZ 10.) Write out 6 completely different reactions of eyclopentanone (reagent, product b) Write out 3 preparations of 3-methyl-1-butanol, a different starting material for each one. In some preps you just have to change the functional group, in other preps you may have to construct the carbon chain. c) Write out 3 preparations of 3-methylbutangle acid, a different starting material for each one. In some...
1.
Write a mechanism for adding the first t-butyl substituent to the
ring. include a teo step electrophile formation and its two-step
displacement of an H
2. Draw the structures of an alkene and an alcohol that coukd
have been used instead of t-butyl alcohol to form
1,4-di-t-butyl-2,5-dimethoxybenzene
3. starting with benzene, an alcohol, an inorganic acids, show
how to synthesize TNT
o LH C(CH₃)₂ а (сн.). Сон OCH3 OCH3 Octs с (сн.) си, 0043 CH3CH2CCH І биз 1 Он
1151 VCL 11-8: Claisen Condensation -1 For this assignment, the target compound that you should synthesize is methyl acetoacetate. This is another carbonyl addition variation. Examine the product and determine which ester is the nucleophile and which is the electrophile. Keep in mind the mechanism and that you need to acidify the intermediate in order to isolate a neutral product. Synthesis Procedures 1. Start Virtual ChemLab and select Claisen Condensation-I from the list of assignments in the electronic workbook. After...
Only need help with 5,6,7
and mechanism
FTIR and NMR Spectra After completing a reaction and working up the products, it is still necessary to confirm that the correct product was formed. The most common tools used for this analysis are Fourier Transform Infrared (FTIR) and Nuclear Magnetic Resonance (NMR) spectroscopy. In the virtual laboratory, 'H and C NMR spectra are available. Details on interpreting FTIR and NMR spectra are found in your textbook. Your instructor may or may not...
I need help with questions 5,
6, & 7. The FTIR and NMR is provided. I also need help creating
a reaction mechanism using the following:
Starting material: methyl acetate.
Solvent: diethyl ether
Reagent: sodium methoxide
Product: methyl acetoacetate
THANK YOU!!!!!
11-8: Claisen Condensation - 1 For this assignment, the target compound that you should synthesize is methyl acetoacetate.This is another carbonyl addition variation. Examine the product and determine which ester is the nucleophile and which is the electrophile. Keep...
What is answer of #10??
Report: Hydroboration of 1-Methylcyclohexene Mechanism / GC Analysis / Calculations 1. After reviewing the GC and 'H NMR spectra, what is the major product of the reaction? + 3 a. BH: . THF 3 b. 3 H2O2 OH + 3 OH c. NaOH MOH OH racemic racemic major 2. Draw the complete curved arrow mechanism for the reaction to produce the major product, including both the hydroboration and oxidation steps. Repetitive steps need only be...
I need help with questions 5, 6, & 7. The FTIR and NMR is
provided. I also need help creating a reaction mechanism using the
following:
Starting material: 1,7-Dimethyl-heptanedioate
Solvent: Diethyl ether
Reagent: sodium methoxide
Product: 3-oxo-cyclohexane carboxylic acid methyl ester
THANK YOU!!!!!
Ö 11-11: Dieckmann Reaction For this assignment, the target compound that you should synthesize is 2-oxo-cyclohexane carboxylic acid methyl ester.This is an intramolecular carbonyl addition variation. Examine the product and determine which ester is the nucleophile and...
What is answer of #9???
Help me
Report: Hydroboration of 1-Methylcyclohexene Mechanism / GC Analysis / Calculations 1. After reviewing the GC and 'H NMR spectra, what is the major product of the reaction? + 3 a. BH: . THF 3 b. 3 H2O2 OH + 3 OH c. NaOH MOH OH racemic racemic major 2. Draw the complete curved arrow mechanism for the reaction to produce the major product, including both the hydroboration and oxidation steps. Repetitive steps need...
Given the NMR and IR graphs, which unknown compound fits your
graph, and fill out the tables about your unknown.
STANDARD 1N OBSERVE Archive directory! Sample directory: F1101 PROTON A 14 Pulse Sequence! s2pul Solvent: CDC13 Ambient temperature Mercury-300BB Hvarian300 Relax delay 1.000 sec Puis 45.0 degrees Acg. time 1.996 sec Width 4803.1 MZ & repetitions OBSERVE NL, 233.9587289 MHZ DATA PROCESSING FT size 32768 Total tine min. 25 sec 2.8 0 ppm 0.94 1604 1081 1364 3063 534 1384...