Identify and analyze the spectral data for Phenacetin and Acetaminophen

Identify and analyze the spectral data for Phenacetin and Acetaminophen, label and integrate (H-NMR) peaks. I'm really bad at NMR 

(for the IR spectra the bottom axis numbers from the left are 4000, 3000, 2000, 1500, 1000, 500)

The Correct Answer and Explanation is :

henacetin and acetaminophen are both analgesic and antipyretic compounds, sharing structural similarities but differing in functional groups.heir proton nuclear magnetic resonance (^1H NMR) spectra provide valuable insights into their molecular structures.
Phenacetin (^1H NMR Analysis):

henacetin (C₁₀H₁₃NO₂) consists of an ethoxy group (-OCH₂CH₃), a phenyl ring, an acetamide group (-NHCOCH₃), and an acetyl group (-COCH₃).

• Aromatic Region (6.5–7.5 ppm): he phenyl protons exhibit a doublet of doublets due to para substitution, with chemical shifts around 7.3 ppm and 7.4 ppm.he downfield shift of the proton near the acetamide group (on C₆,₈) is characteristic of this substitution pattern.citeturn0search16
• Acetamide Group (8.1 ppm): he NH proton appears as a broad singlet at 8.1 ppm, influenced by the nitrogen’s relaxation dynamics.citeturn0search16
• Ethoxy Group (1.4 ppm and 4.0 ppm): he ethoxy group shows a triplet at 1.4 ppm (CH₃) and a quartet at 4.0 ppm (CH₂), indicative of the -OCH₂CH₃ structure.citeturn0search16
• Acetyl Group (2.1 ppm): he methyl group of the acetyl group appears as a singlet at 2.1 ppm.citeturn0search16
  Acetaminophen (^1H NMR Analysis):

cetaminophen (C₈H₉NO₂) comprises a phenyl group and an acetamide group.

• Aromatic Region (6.5–7.5 ppm): he phenyl protons appear as a doublet of doublets, similar to phenacetin, with chemical shifts around 7.3 ppm and 7.4 ppm.citeturn0search1
• Acetamide Group (8.1 ppm): he NH proton appears as a broad singlet at 8.1 ppm, influenced by the nitrogen’s relaxation dynamics.citeturn0search1
  n summary, both compounds exhibit aromatic protons in the 6.5–7.5 ppm range, with acetaminophen lacking the ethoxy and acetyl groups present in phenacetin.he distinct chemical shifts and splitting patterns in the ^1H NMR spectra are crucial for identifying and differentiating these compounds.