(a)
Interpretation:Considering the spectral data for cyclohexanol, to determine any absorptions associated with the alcohol function in the functional group region of the IR spectrum.
Concept Introduction : The analysis of interaction of infrared light with a molecule is termed as infrared spectroscopy. The main use of infrared spectroscopy is identification of
(b)
Interpretation:To assign the various resonances to the hydrogen nuclei responsible for them in
Concept Introduction : Nuclear magnetic resonance (NMR) is a spectroscopy technique which works on the basis that nucleus of the atoms absorbs
(c)
Interpretation:To assign various resonances to carbon nuclei responsible for them in the
Concept Introduction : Carbon-13 NMR has several merits over proton NMR in terms of its power to explain biochemical and organic structures. Carbon-13 NMR provides information related to the backbone of molecules instead of the periphery. In addition, the chemical shift range for Carbon-13 for most organic compound is around 200 ppm related with 10 to 15 ppm for the proton.
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EBK EXPERIMENTAL ORGANIC CHEMISTRY: A M
- Write the reaction involved in Ferrox Test. a. What is the species responsible? b. Why is phenol negative in Ferrox Test? Based on the theoretical result, what is the order of reactivity of primary, secondary, and tertiary alcohols in the Lucas Test? a. Lucas Reagent contains ZnCl2 in HCl. What is the role of ZnCl2? What reagents are used in the esterification of Alcohols and Phenols? a. Write the reaction involved in Primary Alcohol (Ethanol) and Acetyl Chloride b. Write the reaction involved in Phenol and Acetyl Chloride What is the purpose of the Chromic acid test? a. What are the reagents used? b. Write oxidation reaction of Primary Alcohols and Secondary Alcoholsarrow_forwardExplain some of the hazards (name at least three) involved in the (Dehydration of Cyclohexanol – Synthesis of Cyclohexene) experiment. What are some necessary safety precautions when working with sulfuric acid?arrow_forwardSelect a suitable solvent for analysis of one of these terpenes by UV spectroscopy. Explain your choice. Terpenes: Carvone, Carveol, and Pulegone a. ethyl acetate b. benzene c. chloroform d. hexanearrow_forward
- 8. One stereoregular form of polystyrene (A) has a 'H NMR spectrum containing a triplet centered at about 1.4 ppm and a quintet at about 1.9 ppm. Another stereoregular form (B) has an octet at about 1.6 ppm and a quintet at about 2.3 ppm. (Both spectra also exhibit phenyl proton resonances further downfield.) Interpret the spectra and determine which corresponds to isotactic and which to syndiotactic. (Syndiotactic polystyrene was first reported by N. Ishihara and co-workers in a 1986 paper. You may wish to locate the paper and check your answer.)arrow_forwardthis is the spectral data for 4-cyclohexene-cis-1,2-dicarboxylic anhydride 1. Assign the peaks in the region above 1600 cm-1 of the IR. 2. In the 1H NMR spectrum, assign the various resonances to the hydrogen nuclei responsible for them. 3. For the 13C NMR data, assign the resonances to the carbon nuclei responsible for them.arrow_forward4. Suggest two different chemical tests and a major IR frequency that would help distinguish between the following pairs of compounds a. Benzaldehyde and benzyl alcohol b. 2-pentanone and 3-pentanone c. Propanol and diethyl ether d. Propanol and propanoic acidarrow_forward
- Find information on: 1. DDT 2. EDTA 3. orotic acid 4. сarboplatin 2. Propose the approximate shift/splitting pattern/etc. for each type of hydrogen that would be seen in an 'H-NMR spectrum Identify the # of each type of each carbon (i.e. how many peaks in the 13C spectra) 3. Identify infrared (IR) active bonds within each molecule 4.arrow_forwardThe infrared spectrum shown is consistent with which compound? 500 Benzaldehyde a. Ethyl benzoate b. 2-Hexanone C. 4-Hydroxy-4-methyl-2-pentanone d. 1-Hexen-5-one е.arrow_forwardA. In the synthesis of 1-bromobutane, what is the inorganic by-product left in the reaction flask following the distillation? Why was the bromoalkane the bottom layer in the separatory funnel? B. Predict the product when 1-methylcyclohexanol reacts with H2SO4 and KBr. Show the mechanism.arrow_forward
- a. The structure of a standard C4 group chemically bonded to a silica surface through a silyl ether bond. b. A reasonable mechanism by which acid hydrolysis (H* and H20) might cleave the silyl ether bond, including the products of the reaction.arrow_forwardWhich qualitative analysis test from this module can help distinguish between different kinds of ketones? Can this same test give a positive result for 4-methylacetophenone? Why?arrow_forwardAssign the following infrared spectra (Spectrum I and Spectrum II) to a solution of nonanal and acetic acid. Give reasons for your answers. H3C. H3C. TH. nonanal acetic acid Spectrum 1 100 2000 1000 4000 3000 BAVENUERIl 1126 62 1068 57 375 50 866 79 775 84 723 57 676 1 3436 66 2956 10 670 01 S28 81 1467 25 1411 44 1390 1979 70 2926 13 44 41 2872 2856 36 1305 2716 1251 72 1728 10 1146 47arrow_forward
- Macroscale and Microscale Organic ExperimentsChemistryISBN:9781305577190Author:Kenneth L. Williamson, Katherine M. MastersPublisher:Brooks Cole