A molecule of formula C9H10O3 reacts consecutively as shown below to produce the secondary amine. Identify the structure of the C9H10O3 molecule and the material that is produced after the first step.
The given problem is based on the identification of the unknown compound with a given molecular formula from the function of the reagent used. Different functional groups have different functions and attack at a specific position or group.
Reductive amination is an organic reaction in which a carbonyl group is converted into an amine. The intermediate formed in the reaction is imine. Imines are the compounds in which the carbon and nitrogen are doubly bonded to each other.
Sodium cyanoborohydride is a reducing agent similar to , but it is a mild reducing agent due to the presence of electron withdrawing cyano group. It is commonly employed in reductive amination reactions for the reduction of iminium ion.
The structure of sodium cyanoborohydride is shown below:
A general reductive amination reaction is as follows:
The second step of the reaction is follows:
Therefore, the product after the first step is shown below:
The first step of the reaction is follows:
The structure of molecule is shown below:
The structure of the molecule produced after the first step is shown below:
A molecule of formula C9H10O3 reacts consecutively as shown below to produce the secondary amine. Identify...
A molecule of formula C9H10O3 reacts consecutively as shown below
to produce the secondary amine. Identify the structure of the
C9H10O3 molecule and the material that is produced after the first
step.
A molecule of formula C7H12 reacts consecutively as shown below
to produce propyl cyclohexane- carboxylate. Identify the structure
of the C7H12 molecule and the materials that are produced after
each step. Draw only the organic material.
1. Molecule A is a primary amine that was subjected to Hofmann Elimination conditions to produce an alkene. The alkene was then subjected to ozonolysis to produce pentanal and hexanal. Draw the structure of molecule A. No partial credit will be given for this question. 2. Provide a detailed explanation for the observation below. Use drawing and words in your explanation. No partial credit will be given for this question. NH H2SO4 SO3 SO,H
1. Molecule A is a primary amine that was subjected to Hofmann Elimination conditions to produce an alkene. The alkene was then subjected to ozonolysis to produce pentanal and hexanal. Draw the structure of molecule A. No partial credit will be given for this question. 2. Provide a detailed explanation for the observation below. Use drawing and words in your explanation. No partial credit will be given for this question. NH2 H2SO4 SO3 SOZH
Molecule A is a primary amine that was subjected to Hofmann Elimination conditions to produce an alkene. The alkene was then subjected to ozonolysis to produce pentanal and hexanal. Draw the structure of molecule A. No partial credit will be given for this question. 1. 2. Provide a detailed explanation for the observation below. Use drawing and words in your explanation. No partial credit will be given for this question. NH2 NH2 H2SO4 So3 soH
Identify each functional group shown in bold letters. For each molecule shown below: 1) circle any bonds which have considerable polarity, 2) Indicate which atoms arc positive or negative, and 3) tell whether or not the overall molecule is polar The infrared spectrum of a molecule shows peaks at 3000, 1700, 1400 and 1200 cm^-1 Which of the molecules drawn in Part 3 would produce this spectrum? Explain how you made your choice. List each of these halides as primary,...
Consider the information given below and identify the structure of the unknown compound A, with a molecular formula of C8H14. Compound A reacts with Br2/CCl4. Upon reaction of A with excess H2/Ni, 1-ethyl-2-methylcyclopentane is produced. Subjecting A to ozonolysis, the product shown below is produced as the major organic product. Draw the correct structure of compound A, and provide a brief and clear explanation relating the data provide with the structure selected.
of the 15) 4. Show a sequence of reactions that will produce the molecule shown below, starting with ethyne as the only organic starting material. Any other organics used must be made from ethyne, but you can use any inorganic reagents or solvents
5 a) identify the anomeric carbon in the below molecule
b) identify the thpe of ring pyranose or furanose
c) identify if it is a or b
6 a) identify the anomeric carbon in the below molecule
b) identify the thpe of ring pyranose or furanose
c) identify if it is a or b
7 The structure of 6-carbon ketose sugar is shown. Draw the
common cyclic structure of this structure (both a and b form)
8 Identify the relationship...
1.(a) (2pts.) Draw the structural formula for each amine. (b) provide the IUPAC name the structure below 4-aminobutanal (R)-2-butanamine 2. (6 pts.) Consider the Grignard reaction shown below which forms a C-C bond via an Aw step. In box A, draw the structure of the nucleophile involved in the A step and highlight the nucleophilic atom. In box B, draw the structure of the electrophile involved in the Aw" step and circle the electrophilic atom. In box C, draw the...