Draw the structure(s) of the ketone(s) with the molecular formula C5H10O that contain a 5-carbon chain.
Draw the structure(s) of the ketone(s) with the molecular formula C5H10O that contain a 5-carbon chain.
Using the IR and 1H NMR spectra, draw a deduced structure. The molecular formula is C5H10O lUnhula is CsHio0 and the spectra are given below 0 ppm SD 1000 1500 4000
Draw dash formula structure of a 5-carbon compound (may be branched or straight chain; and multiple possibilities) with the following functional group: (a) Alkane (b) Alkene (c) Alkyne (d) Alcohol (e) Aldehyde (f) Ketone (g) Ester (h) Nitrile
Draw a structural formula for one of the three ketones with molecular formula C5H10O.
Deduce the structure of the compound with molecular formula C5H10O. Deduce the structure of a compound with molecular formula C_3 H_10 O that exhibits the following IR, H^2 NMR, and C^13 NMR spectra. Data from the mass spectrum are also provided.
A compound with a molecular formula C5H10O has the following 1H NMR spectrum. Provide a structure that is consistent with this spectrum. 3. A compound with a molecular formula CsHioO has the following 'H NMR spectrum. pound with a molecular formula CsHioO has the following H NMR Propose a structure for this compound. PPM
Draw the skeletal structure that fits the following descriptions. a. an amine with the molecular formula C4H8N b. a molecule with the formula C5H6 that has both alkene and alkyne functional groups. c. an ester with 2 sp2 carbons d. a molecule with molecular formula C6H11Br that has an electrophilic carbon. Label that carbon e. a molecule with the same carbon backbone but that will have slightly higher boiling point than CH3CH2CH(OH)CH2CH3 f. Acid halide functional group with C3H5OCl molecular...
Draw at least four constitutional isomers (using bond-line/skeletal representations) with the molecular formula C5H10O. Make sure that each constitutional isomer has a different functional group present.
Please fill out charts:) Determine the structure of the ketone with molecular formula C_6H_12O giving the^1H NMR below and finish the table Draw the structure of the molecular fragment that corresponds to the given^1H NMR data 2 points. [1H] no net at 1.3 ppm [2H] quartet at 2.1 ppm
5. Draw the structure of an ether with molecular formula C. H of an ether with molecular formula CH.. that is the following NMR spec O , that fits the CHUO, O 0.5 00 -0.5 6. Draw the structure of an ester with molecular formula C H 40, that fits the following NMR spectrum. CHO 2.00 95 2.96 6.01
5) Draw 3 isomers with the molecular formula C6H14 that do NOT contain a stereocenter Below each molecule, indicate: (i) the degrees of unsaturation (2), (ii) number of signals in the C-NMR spectrum, and (iii) number of signals in the 'H-NMR spectrum. Be sure to properly label awarded. For example you could format your answers below each structure 13 or credit will not be