Name the following compounds according to the IUPAC system. (i) (ii) Draw out of structures for...
Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC name of the following compounds: CHCH2 a CHCH2 II III 2) Drawing Structures Methylenecyclohexane Trans-3,3-dimethyl-4-propyl-1,5-octadiene (3Z,SE) -26-dimethyl-1,3,5,7-octatetraene 4-methyl-1,2-hexadiene
Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC name of the following compounds: WHICHCH2 at CHCH2 II III 2) Drawing Structures Methylenecyclohexane Trans-3,3-dimethyl-4-propyl-1,5-octadienc (3Z,SE) -2,6-dimethyl-1,3,5,7-octatetraene 4-methyl-1.2-hexadiene
2. Draw structure (or) name the molecules according to IUPAC rules. (10 pt) i. 2,6-dimethyl-5-propyloctane Name the following compounds according to IUPAC nomenclature. ii. E: CH.CH C(CH3) 3. Give five different structures of CH3 alkyl groups, and identify the carbon at the point of attachment as primary, secondary or tertiary as appropriate. (10 pt)
1. Name the following Compounds (1 Point Each) i. IUPAC Name ii. Common Name i. IUPAC Name ii. Common Name
VL Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC name of the following compounds: CHCH2 CHCH Il III 2) Drawing Structures Methylenecyclohexane Trans-3,3-dimethyl-4-propyl-1.5-octadiene 4-methyl-12-hekadiene (3ZSE) -2,6-dimethyl-1.3.5.7-octaterne
1. Name the following compounds using the IUPAC system. No stereochemistry designations needed. (16) b yo thy d. 2. Draw two resonance structures of the anion formed from the following acid-base reaction. (4) y + NaOH
Draw correct. condens Cyclic portions of structures condensed structures for the following compounds according to IUPAC rules portions of structures can be done as line-angle drawings (20 pts.) b) |-ethyl-2-methylcyclohexane a) 1.1.2-trichloro-2-fluoropropane d) cis-4,4,5,5-tetramethyl-2-hexene 3-ethyl-2,2,3-trimethyloctane 3,3-dimethyl-1-octyne 4-ethyl-2-heptene 8) 1-chloro-2-propyleyelopropane h) 1,2,4-tribromo-3-chlorocyclohexane i) trans-4-ethyl-2-octene i) 1-bromo-1-chlorocycloheptane 3) hake 1-bromopentane as the only product from the reaction of 1-pentene with Can you easily make 1-bromopentane as the HBr and why? (Explain!) (10 pts.) (HINT: You may want to draw out a chemical...
1. Name the following compounds using IUPAC or accepted common name: 2. Draw a proper condensed, expanded or line-angle structures for the following compounds: /8 a. hepta-1,4-diyne b. cis-non-2-en-5-yne c. trans-6-chlorohept-2-en-4-yne
1. Name these compounds according to the IUPAC system Include stereochemistry (cis/trans, EIZ) where shown. a) oL 2. Write "most under the alkene which is most stable. Write "least" under the alkene which is least stable.
Give the IUPAC name for the following structures: Part II: Give the IUPAC name for each of the following structures. (10 marks) 1. нс. CH CH3 CH3 2. нс. CH3 CH3 CH3 3 -CH3 CH3 CH3 4. F CH3 CI 5. À 6. HC CH3 Br CH3 H 7. H 8. H3C 9. HC CI HC CHE 10. H3c CH3