(A) 86α ULLE 58 72 60 Relative intensity 100- 15 m/z 20 40 80 100 114a Cattato co C3HCH₂N(CH3) 129M+. 120 86 CH3 H CH3 1143 140

Q: C3H1,0 5H 2H 2H 1H 8 6 3 PPM

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A:

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A:

Q: Compound 4: C3H13N 11 10 8 7 6 5 4 2 1 m(1 H) s(6 H) d(6 H) 200 180 160 140 120 100 80 60 40 20…

A: Given:  Molecular formula= C5H13N  From proton spectra: 3 types of Hydrogens From carbon spectra: 3…

Q: Which of the following would not show a C-C signal in an IR spectrum? CI CI CI CI

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Q: Spectrum 7 Relative intensity 100 80 60 40 20 MS-NW-3920 pwypo 10 20 30 40 50 1|tq||||||| 70 60 m/z…

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Q: I 200 I 0 120 100 PPM | || ||| IV

A: P

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Q: Compound 4: C5H13N lle 11 10 8 7 6 4 2 m(1 H) s(6 H) d(6 H) 200 180 160 140 120 100 80 60 40 20 ppm…

A:

Q: pectrum 7 OD 50 D 4000 3000 mportant Peaks: Wavenumbers:_ ame of compound: 2000 HAVENUMBERI-I way…

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Q: 4.0 H₂C I 3.0 11 H₂ CH3 I CH CH3 III IV 2.0 ppm 1.0

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Q: D 50 D 4000 3000 2000 1500 1000 5 00 HAVENUMBERI -il

A: 1 . Strong and Sharp peak at 2250 cm-1 (CN) . 2. Weak band at 2950-2840 because of CH stretch.

Q: Spectrum 2: LOD 4000 3000 2000 1S00 1000 HAVENUMBERI -l

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Q: 100 50 15 -8 41 57 68 81 85 (96) т OH н+ 1914+.

A: G

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Q: How many signals would be in a CNMR AND HNMR for this product? Please explain in depth.

A: Step 1: Step 2: Step 3: Step 4:

Q: Three students examined the signals in the HNMR spectrum shown below. The first student concludes…

A: Doublet and quatrate peaks are like this