formulate a mechanism for the following problem. 3. Formulate a mechanism for the formulation of acetamide,CH-CO-NH,,...
formulate a mechanism using methyl acetate and ammonia to form acetamide? (arrow pushing shown)
please help a. C. CH-CNH Which of the following is alanylglycine? O O *NH-CH-C-NH-CH-CO H CH, b. о NH-CH-C-NH-CH-CO- CH CH,OH d. NH-CH-C-NH-CH-CO- CH, H O O 요 *NH-CH-C-NH-CH-CO CH,OH CH NH,CH-C-NH-CH CH-C
A chemical engineer is studying the following reaction: HCH,CO (0)+CH NH (aq) – CH, CO (q) + CH3NH (g) At the temperature the engineer picks, the equilibrium constant for this reaction is 2.2. The engineer charges ("fills") four reaction vessels with acetic acid and methylamine and lets the reaction begin. He then measures the composition of the mixture inside each vessel from time to time. His first set of measurements are shown in the table below. Predict the changes in...
NH₂ (CH 3 CO), ? HNO₃ A B Pyridine H₂SO4 ] and neat What products are I and B? NH₂
Br 3. Show complete mechanism and intermediates formed in the following Sel process. OH + H ő heat ОН minor major 4. Determine if Sylor Sw2 mechanism is likely to take place based on conditions and show products for the following reactions. 1. 1-bromohexane reacting with sodium cyanide in acetonitrile (CH3CN) 2. tert-butyl iodide reacting with sodium acetate (CH3CO,Na) in acetic acid (CH,CO,H) 3. (S)-2-iodobutane reacting with potassium acetylide (NaC,H) in tetrahydrofuran 4. 1-bromo-1-methyl-cyclohexane reacting with water at 95°C.
What is the correct name for the following compound? d) 5-oxo-3-octenoic acid What is the defining functional group of a carboxylic acid? a) an-H attached to a carbonyl group b) an-H attached to a carbon-carbon triple bond c) an-OH attached to a carbonyl group d) an -OH group attached to a O-C double bond e) an-OH group attached to an aromatic ring To convert a carboxylic acid to an aldehyde a) convert the acid to an acid chloride, then use...
Homework Problems 9.1 Give the name for each of the following: COOH CH, c. CHE-CH-CH2-COOH d. (CH CH),CCOOH 9.2 Draw the structural formula for each of the following compounds: a. sodium hexanoate b. potassium acetate c. zinc benzoate d. calcium propanoate 9.3 Complete the following reactions: a. CHỊ– –OH + CH3CH-CH-OH " b. (CHỊ) CCH-CH-COOH + (CH, CHOH | COOH + CH CH OH d. CH (CH),COOH + 9.4 Draw a structural formula for each of the following esters: a....
please the problem solution... (b~c) what products?? b. Intramolecular CO migration OC-Me FS CH, If the mechanism were the reverse of intramolecular CO migration, the CO lost would be cis to the acyl group: (1) Loss of CO from position 1: (2) Loss of CO from positions 2 & 3: c. Intramolecular CH, migration CM- CH If the mechanism were the reverse of intramolecular CH, migration, the products would be (1) Loss of CO from position 1: Product A (2)...
MMM Page E 21 Which arrow designates the bond broken by hydrolysis? O “NH CHÚC-NH-CH-CO- A CH S S DO CH, *NHẠCH CẠNH-CH-CO- a. b. (A) (E (C) (D) 22 a. 23 The following side chain occurs in which amino acid? CH.CH.CH_CH_NH, alanine b. glutamic acid c. cysteine d. lysine Classify the following carbohydrate. aldotetrose CHO b. aldopentose c. ketopentose H-COH d. ketohexose ketotetrose H-C-OH a. HO-CH 24. CH,OH Which of the following always undergo hydrolysis reactions? (There may be...
Propose a mechanism from the reaction in the box CH,CH,0 + NH CH:CH-OH + NH3 Use the diagram above for Questions 4-7. 4. Which reactant is the base? a) CH3CH20 b) NHÀ c.) CH,CHOH d.) NH3 5. Which product is the conjugate acid? a.) CH CH20 b.) NH4+ c.) CHCH2OH d.) NH3 6. Which reactant is the acid? a.) CH,CH20 b.) NHÀ c.) CH3CH2OH d.) NHS 7. Which product is the conjugate base? a.) CH,CH20 b) NH4* c.) CH,CH2OH d)...