The MCPBA is used in the epoxidation of alkanes, at the carbon carbon double bond there occurs epoxidation. So the structure I represents the correct reaction product.
Question 1 1 pts The alkene shown below reacts with meta chloroper benzoic acid (MCPBA) in...
The alkene shown below reacts with meta-chloroperbenzoic acid (MCPBA) in tetranyarului DIL VICITU LIIC TOUTUMU describe the reaction products? = = оооо = =
The reaction of the alkene shown below with hydrobromic acid generates the four stereoisomeric products shown below. Provide an electron-pushing mechanism for this reaction that shows the generation of one of the products depicted. HBr . . . .
Question 7 1 pts What type of functional group is shown below? NH2 Alkyne Alkene Amine Carboxylic Acid Alcohol Ester Amide
2. Compound A reacts with E+ to form the ortho and meta intermediates shown below. ENN Orice om contato M1 M2 The least stable intermediate is ___, which tells me the CN group is a director. Check two (2) boxes. N 01 (blank 1) O O 02 (blank 1) 03 (blank 1) 04 (blank 1) M1 (blank 1) M2 (blank 1) M3 (blank 1) M4 (blank 1) O ortho, para (blank 2) O meta (blank 2)
Experiment 12: Synthesis of Benzoic Acid pre-lab (4 pts) 1 (2 pts) Refer to the introduction on the general process of hydrolysis of nitriles to carboxylic acids. Starting with benzonitrile (shown below), show how it is converted to benzoic acid under basic conditions. N 2) (2 pts) The reaction for the synthesis of benzoic acid via benzonitrile hydrolysis is shown below: 1) NaOH, HO YOH + NaCl 2) HCI, H,0 Benzonitrile Density = 1.0 g/mL MM = 103.04 g/mol Benzoic...
show all work please thank you!!! 3. (10 pts total) Consider the following alkene addition reaction: Brz H2O НО Br a. (3 pts) This type of alkene addition reaction is mediated by both Lewis acids and bases. Of the two inorganic reactants (Br2 and H2O), place a triangle (1) around the one which functions as a Lewis acid in the above transformation b. (3 pts) of the two regioisomeric reaction products shown, only one is observed to form under the...
QUESTION 1 Propanoyl chloride reacts with an acetate anion to give which product? Acetic propanoic anhydride propanoic acetic anhydride propyl acetate Cacetyl propanoate QUESTION 2 Reaction of benzoic acid with thionyl chloride produces compound A. Compound A is reacted with 2 moles of ammonia to give compound B which is then reacted with thionyl chloride to furnish compound C. Compounds C is then treated with NaOH in the first step and acidified with acid in the second step to give...
0 Question 4 6 pts The rate determining step in the bromination of an alkene creates a bromonium ion. Which of the structures drawn is correct for the intermediate in the reaction shown? (+/-) :Br: Question 5 6 pts How many asymmetric centers (ie, stereocenters) are present in the compound shown below?
The alkene shown below is treated sequentially with ozone (O3) and zinc/acetic acid. Draw structural formula(s) for the organic product(s) formed. The alkene shown below is treated sequentially with ozone (03) and zinc/acetic acid. Draw structural formula(s) for the organic product(s) formed. CH3CH2 C=CHCH2CH3 CH3CH2 • You do not have to consider stereochemistry. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate multiple products using the + sign from...
Question 2 (25 pts.) This is benzoic acid. Draw MINOR RESONANCE contributors as necessary to explain why the nmr chemical shift of carbon A is larger than that of carbon B. Give a brief explanation that includes the terms "deshielding" and "electron density. Question 3 (18 pts.) Rank the indicated hydrogens A, B and C in order of INCREASING chemical shift, give a BRIEF explanation. You do not need to invoke resonance to answer this question. lowest highest Question 4...