How would I draw the abbreviated structural formulae of the products of the complete hydrolosis of this compound,

CH3 O
(=)
N - C - CH - NH2
(-) (-)
H CH3

CH3

Sorry about the drawing, the bonds in brackets should be vertical, thanks.

We simply can't draw structures on the board. Sorry.

No problem! I understand that it's difficult to draw structures on text-based platforms. However, I can still explain how to determine the abbreviated structural formulae of the products of the complete hydrolysis of the given compound.

To get the abbreviated structural formulae of the products, you need to know how the hydrolysis reaction occurs. Hydrolysis is a chemical reaction that involves the breaking of chemical bonds in the presence of water. In this case, the hydrolysis process will break the bonds between the atoms in the given compound and replace them with hydroxyl groups (-OH) from water.

Let's break down the given compound, step by step, to identify the possible hydrolysis products:

CH3 O
(=)
N - C - CH - NH2
(-) (-)
H CH3

The compound consists of several functional groups, namely a methyl group (-CH3), an ether group (-O-), an amide group (-CONH-), and an amine group (-NH2). We will separate each functional group to analyze their individual reactions during hydrolysis.

1. Methyl Group: The methyl group (-CH3) is not typically reactive in hydrolysis reactions. Therefore, it will likely remain unchanged in the hydrolysis process.

2. Ether Group: The ether group (-O-) can undergo hydrolysis to produce an alcohol (-OH) group on each end. In this case, the hydrolysis would yield two hydroxyl (-OH) groups.

3. Amide Group: The amide group (-CONH-) can undergo hydrolysis to produce a carboxylic acid (-COOH) and an amine (e.g., -NH2) group. So, in this case, the hydrolysis of the amide group would yield a carboxylic acid and an amine.

4. Amine Group: The amine group (-NH2) would not typically undergo hydrolysis, and it will likely remain unchanged in the reaction.

Based on this analysis, the abbreviated structural formulae of the hydrolysis products would be as follows:

CH3 O
(=)
N - C - CH - NH2
(-) (-)
H CH3

After hydrolysis:

1. The methyl group (-CH3) remains unchanged:
CH3 O
(=)
N - C - CH - NH2
(-) (-)
H CH3

2. The ether group (-O-) would be hydrolyzed into two hydroxyl groups (-OH):
CH3 OH
(=)
N - C - CH - NH2
(-) (-)
H CH3 OH

3. The amide group (-CONH-) would be hydrolyzed into a carboxylic acid (-COOH) and an amine (-NH2) group:
CH3 OH
(=)
N - C - CH - NH2
(-) (-)
H COOH + NH2

Please note that without specific information about the groups attached to the amine and the carboxylic acid, I have used generic letters (R groups) for them.

I hope this explanation helps you understand how to determine the abbreviated structural formulae of the hydrolysis products. Let me know if you have any further questions!