Answer:
The simulated 1H NMR spectrum for ethyl acetate is shown in the drawing attached.
Explanation:
To construct this NMR it is necessary to identify the essential components that can produce resonance peaks.
Two main groups can be identified, the acetyl group containing a sub-component (CH3) capable of producing a resonance peak, and the ethyl group containing two components (CH2 and CH3) each of which can produce on its own its own resonance peak.
The question is incomplete, complete question is :
In an organic structure, you can classify each of the carbons as follows: Primary carbon (1°) = carbon bonded to just 1 other carbon group Secondary carbon (2°) = carbon bonded to 2 other carbon groups Tertiary carbon (3°) = carbon bonded to 3 other carbon groups Quaternary carbon (4°) = carbon bonded to 4 other carbon groups How many carbons of each classification are in the structure below? How many total carbons are in the structure? How many primary carbons are in the structure? How many secondary carbons are in the structure? How many tertiary carbons are in the structure? How many quaternary carbons are in the structure?
Structure is given in an image?
Answer:
There are 10 carbon atoms in the given structures out of which 6 are 1° , 1 is 2° , 2 are 3° and 1 is 4°.
Explanation:
Total numbers of carbon = 10
Number of primary carbons that is carbon joined to just single carbon atom = 6
Number of secondary carbons that is carbon joined to two carbon atoms = 1
Number of tertiary carbons that is carbon joined to three carbon atoms = 2
Number of quartenary carbons that is carbon joined to four carbon atoms = 1
So, there are 10 carbon atoms in the given structures out of which 6 are 1° , 1 is 2° , 2 are 3° and 1 is 4°.
