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based on the following H NMR and C NMR determine which acid is present: 2,5- dichlorobenzoic...

based on the following H NMR and C NMR determine which acid is present:

2,5- dichlorobenzoic acid
2,4,6- trimethylbenzoic acid
3-chlorobenzoic acid
3-hydroxybenzoic acid
2-iodobenzoic acid

7.3464 7.3243 7.3184 7.2563 See all 180 177.3251 Bean, Klimabeth EM ACID21 166.5565 160 CNMR Acid 140 140.0977 135.1928 d
HNMR - Acid Bean irabeth NEW ACID 5:\n\data\chnos\sep spec Mall 2019 section helda 6.8593 6.8414 6.8025 6.7786 6.7520 15 1
7.3464 7.3243 7.3184 7.2563 See all 180 177.3251 "Bean, Klimabeth EM ACID"21" 166.5565 160 C'NMR Acid 140 140.0977 135.1928 datalos Bep_Spee Fall 2017 Section Aids - 123.5895 121.8342 120 117.5069 100 110-110 = Benene Ring 80 (ppm] CDCI 82.3304 81.9045 81,4789 50 fred
H'NMR - Acid Bean irabeth NEW ACID" "5:\n\data\chnos\sep spec Mall 2019 section helda 6.8593 6.8414 6.8025 6.7786 6.7520 15 10 N 0.9832 1.0000 0.0556W 0.9573 1.0487 7.5 6.5 ppm] 5 Hydrogen Types
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From 13C spectra, all the 6-aramatic carbons appears at seperate chemical shift indicate unsymmetrical struture. V OH only th

HNMR - Acid н. на о кон residual solvent peak from CDCI, 5 Hydrogen Types

All the chemical shifts are assigned based on the coupling pattern and roofing effect as observed.

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