4. Draw the structure for each compound. a. 2 chloroaniline b. 3,5-dichloroaniline S. Name each compound. b. CH,CHNHCH, CH CHICHCH,CH,CH, NH, 6. Name each compound 7. Draw the structure for each compound. a. dimethylammonium chioride b. anilinium chloride ure for each compound uraw the struct methylammonium chloride b. anilinium nitrate 9. Name each compound 10. Name each compound.
2. Below are the aromatic regions for the proton NMR spectra for four isomers of dimethoxybenzaldehyde. These isomers are: 2,4-dimethoxybenzaldehyde, 2,5-dimethoxybenzaldehyde, 2,6-dimethoxybenzaldehyde, and 3,4 dimethoxybenzaldehyde. Draw the structure responsible for each spectrum in the box to the right of the spectra. To help in solving this problem, remember that aldehyde groups are electron withdrawing through resonance. Therefore, nearby protons would be deshielded. On the other hand, methoxy groups are electron donating through resonance. Therefore, nearby protons would be shielded. (10...
1. provide the IUPAC name and draw for the following compound . (CH3)3CCCH(CH3)2 2. draw an acceptable structure for 3-hexyne. 3. draw the structure for the following compound. (3Z,5E) 4-methyl-3,5-nonadiene
2. Draw a stereochemically correct structure for (S,3Z,5E)-7-bromo-2,3,5,6-tetramethylnona-3,5-diene?
2. Draw a stereochemically correct structure for (S,3Z,5E)-7-bromo-2,3,5,6-tetramethylnona-3,5-diene?
Draw the structure of the reaction between NaOCH3 and the following compound in methanol Draw the structure of the reaction between NaOCH3 and the following compound in methanol
Draw the structural formula of (3Z,5E)-4-methyl-3,5-nonadiene Mastering Chemistry HW 06-Chapter 5 Nomenclature: Draw the structure of (3Z,5E)-4-methyl-3,5-nonadiene Part A Draw the structural formula of (3Z,5E)-4-methyl-3.5-nonadiene. H O
15.1 Draw a structure for the compound named below. O-nitroanisole 15.1 Draw a structure for the compound named below. NO₂ NO₂ NO (a) (d) OCH, OCH3 „NH2 NH₂ 2 (b) (e) OCH3 OCHZ NO2 NO2 () "NH2 NH2 a co С e Сf
Draw the structure of Compound A based on its formula and proton NMR. The integration of the peaks from left to right is: 5:2:1 Compound A MF C_7H_8O Draw the structure of Compound B. Draw the structure of Compound C.
Draw a mechanism for a green aldol synthesis without solvent. using 3,4-dimethoxybenzaldehyde, 1-indanone, NaOH, HCl, ethanol and water