4. Draw the structure for each compound. a. 2 chloroaniline b. 3,5-dichloroaniline S. Name each compound....
1) Draw the structure for each named compound: a) (Z)-N-ethyl-3-bromo-2-isopropyl-5- b) propanoyl chloride methyl-2-hexenamide c) benzoic anhydride d) (R)-3-chloro-4-ethylhexanoic acid e) ethyl 4-methylpentanoate f) pentanenitrile g) cyclohexanecarboxamide h) octyl butanoate 2) Provide an IUPAC name for each structure: b) 9 CH d) CH.CH нс снсон TH Page
4) Which structure is consistent with this IR spectrum? 2.5 27 3 3,5 Wavelength, (um) 4 4,5 5 5,5 6 6,5 7 8 9 10 12 14 18 4000 3500 3000 2500 2000 1800 1600 1400 12001000 800 600 400 Wavenumber, (cm) (A) (B) CH3(CH2).CH OCCH; CHCH).CH_OČCH, B) ChọCh> OH CH(CH2) 10COH (C) CHCH_CHE (D) HOCH_CH»ČCH, 5) Which compound corresponds to this IR spectrum? 1 2.527 3 3,5 Wavelength, (um) 4 4,5 5 5,5 6 6,5 7 8 9 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
Draw Lewis structure and show the lone pairs on each ce 1. NH, 2. NF one pairs on each central atom for the following species: 3. NH+ 4 H.O 5. BF: 6. XeF. 7. BrFs 8. PCI 9. ASF 10. CH Experiment 12-Molecular Geometry & Bondins
Compound A Compound B Give the IUPAC name for Compound A. 2. Give the IUPAC name for Compound B. 3. Which compound from above (Compound A or Compound B) is more soluble in water and why? 4. Which compound can be dehydrated to form a double bond (Compound A or Compound B)? Draw the most likely product of that dehydration. (Insert a picture of your drawing of the molecule or a scan of your drawing of the molecule) 5. Could...
Name the structure using the IUPAC system. Please explain.
a) 3,5-methyl-4-ethylheptane
b) 2,3-diethyl-4-methylhexane
c) 3-butyl-4-methyl-hexane
d) 4-ethyl-3,5-dimethylheptane
CH3 CHCH2 CH3 CH3 CH2CHCH CH2 CH CH3
1. Give the correct name for each compound. 2. Determine the degree of unsaturation for the molecular formula, C.H.BrCl. Draw and name at least five isomers for the above molecular formula. 3. Draw a structure for each compound. (a) (E)-2-chloro-2-hexene (b) (3,6Z)-1,3,6-octatriene (c) trans-3-methylhept-3-ene 4. Predict the elimination product(s) formed by debromination of the following compound with iodide ion in acetone. Include stereochemistry, and give a correct name for the product. B -CH₃ "Br + Acetone r A CH₂ 5....
2) Which is the most reasonable structure for a compound with this IR spectrum? Wavelength, (um) 2.2 2.4 2.6 3 3,5 4 4,5 5 5,5 6 1 8_9 10 11 12 13 14 16 MAN 4600 4000 3500 3000 2500 2000 1500 Wavenumber, (cm) 1000 800 600 (A) (B) ОН CH3(CH2)4-C=C-COCH; CH(CH2)3-C=C-CHCH (C) (D) H-C=C-(CH2)4CCH3 CH3(CH2)4-CH=CH-CH 3) Which structure is consistent with following IR spectrum? * 2.527 3 Wavelength, (um) 3,5 4 4,5 5 5,5 6 6,5 7 8 9...
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?