Below is a DEPT-135 spectrum for compound D. Identify a structure for compound D that is consistent with the data in the spectrum. Compound D-DEPT 135 90 H3C 70 CH3 CH 50 30 10 8 (ppm) CH₂CH₂CH-C1 CH3 CH3CH₂CH₂CH₂-Cl CH3 CH3-C-CH3 Cl
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- The 1H and 13C NMR spectra of compound A, C8H9Br, are shown. Propose a structure for A, and assign peaks in the spectra to your structure.The 'H NMR spectrum of compound A (C3H100) has four signals: a multiplet at 8 = 7.25-7.32 ppm (5 H), a singlet at d = 5.17 ppm (1 H), a quartet at d = 4.98 ppm (1 H), and a doublet at ô = 1.49 ppm (3 H). There are 6 signals in its 13C NMR spectrum. The IR spectrum has a broad absorption in the -3200 cm-1 region. Compound A reacts with KMNO4 in a basic solution followed by acidification to give compound B with the molecular formula C7H6O2. Draw structures for compounds A and B.Compound B has molecular formula C9H12. It shows five signals in the 1H-NMR spectrum - a doublet of integral 6 at 1.22 ppm, a septet of integral 1 at 2.86 ppm, a singlet of integral 1 at 5.34 ppm, a doublet of integral 2 at 6.70 ppm, and a doublet of integral 2 at 7.03 ppm. The 13C-NMR spectrum of B shows six unique signals (23.9, 34.0, 115.7, 128.7, 148.9, and 157.4). Identify B and explain your reasoning.
- A ¹H NMR spectrum is shown for a molecule with the molecular formula of C10H12O4. Draw the structure that best fits this data. 1H 11 10 2H 2H U 7 1H 1H ΤΗ 1Η ppm QAssume that you have a compound with the formula C4H8O. a) How many double bonds and/or rings does your compound contain? b) If your compound shows an infrared absorption peak at 1715 cm-1, what functional group does it have? c) If your compound shows a single 1H NMR absorption peak at 2.1 δ, what is its structure?5. Determine the structure of a compound with a molecular formula of C4H8O2 with the 13C and 'H NMR spectra below. No peaks exchange with D20 on the 'H NMR spectrum. ada I=2 |=3 1=3 1.2 4.0 4.0 3.0 2.0 1.0
- A compound has the molecular formula: C4H8O2 and gives the following C-13 NMR spectrum. Provide the most likely functional groups for each signal. nmrsim presentation 1 1 C:Bruken Topspin3.5pl7 examdata -170.7658 150 100 d 170.8 (O CH3) ; 60.4 (OCH2); 20.8, 14.1 (2 x C=0) 8170.8 (0 CH₂); 60.4 (OCH₂); 20.8, 14.1 (2 x CH3). 8 170.8 (CH3); 60.4 (C-0); 20.8, 14.1 (2 x OCH₂) 8170.8 (C=0); 60.4 (OCH₂); 20.8, 14.1 (2 x CH3). 8170.8 (C) ; 60.4 (O CH2); 20.8, 14.1 (2 x O CH3) -60.4293 50 -20.7902 -14.1385 [ppm] [+]These are the 1H RMN and IR spectrums of an A compound with formula C10H13NO2. When A reacts with NaOH in water and heat, B compound is formed, with formula C10H11NO. What are the structures of A and B?G 8 HR201403000NS 18) The partial chemical structure and ¹H NMR spectrum of a compound with the formula C4H10O. Determine which of the following structures fit the spectrum (A-D). Provide a brief rationalization of the structure. 4H B) Peak 1: Peak 2: () HE 3.47 ppm 1.21 ppm 6H Triplet D) XOH I 0 Quartet ppm A) 4 Identity of Unknown: Explanation: WASTOR SERVICES FOR CHILDREN&FAMILIES wwww..
- The following is the predicted H-NMR spectrum for an unknown compound with molecular formula C6H140. This compound is a liquid at room temperature, is slightly soluble in water, and reacts with sodium metal with the evolution of a gas. 5 6H 2 2H 4H 1H 1H PPM Choose from the constitutional isomers below to assign a structure to this spectrum. e f b a CH3 CH2CH3 CH3 CH;CH,CH,CHCH,OH CH,CH,CHCH,OH CH;CH,CHCHCH, b| d CH3CH2CH2CHCH2OH CH3CH2ČHCH2OH a b c deg a a b c de OH f А B C (Choose the letter corresponding to the correct structure from the drop-down list provided.) Correct Structure: Assign signal number 5 (indicated as a red number on the spectrum above) to the corresponding hydrogen(s) (shown as a red lower-case letter on the structure above). If relevant, consider the possibility of diastereotopic hydrogens with slightly different chemical shifts. (Write the letter(s) of the hydrogen (or set of equivalent hydrogens) in the box provided. If the signal arises from more than one set…identify the compound with molecular formula C2H6O that gives this 1H NMR spectrum.Compound X (molecular formula C10H120) was treated with NH2NH2, ¯OH to yield compound Y (molecular formula C10H14). Match the 1H NMR spectra of X and Y to the corresponding structures of X and Y. Compound NH2NH2 Compound 'H NMR of X 6 H OH Y 1 H 5H 8. 6. 4 ppm or H NMR of Y 6 H 2H 5H 1 H multiplet multiplet 8. 6. 4. 3. 1 nnm 2. 2. 3, O: