Provide IUPAC names for the following molecules: CH2CH2 - Draw structures (diagram) from the following names:...
1. Provide IUPAC names for the following molecules: CH,CH2 Y 2. Draw structures (diagram) from the following names: a) 3-propyl cyclopentene b) (2)-2-bromo-3-methyl-2-heptene 3. Provide a step-by-step mechanism for the following reaction: 4 - t
Provide IUPAC names for each of the following structures: Draw structures corresponding to each of the following names: 6. 2-propenamide 7. 3,4,5-trimethoxybenzoyl chloride 8. acetic formic anhydride 9. N,N-dimethylformamide 10. methyl cis-3-ethylcyclobutanecarboxylate 11. (E)-2,4-dimethyl-2-hexenoyl chloride
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
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
15 points) Provide the mechanism for the following reaction. For proton transfer may use H-A for a generic (non-specific) acid, or B: as a generic base. Question 5 (15 p steps, you may use od odt.de Question 1 (6 points). Provide IUPAC names for the following structures, Question 2 (14 points). Convert the following IUPAC names into structures. 2,4-dimethylcyclopent-2-enone 5-hydroxy-2-phenyl-3-hexanone (S)-2-bromo-2-methylcyclobutanone 3-methyl-5-(4-chlorophenylhexanal 3-isobutylbenzoic acid Acetic butanoic anhydride N-phenyl-N-propyl-2,3-dimethylbutanamide
2. Draw structures corresponding to the following IUPAC names a. 2-methy-1,J-hexadiene b. (Z)-3-ethyl-2,2-dimethyl-3-heptene a. Z-me c. 3.4-diisopropyl-2,5-dimethyl-3-hexene d. (E)-5-methyl-4-hepten-2-ol
4. Draw the structures and provide the IUPAC names of the two allylic monohalogenation products of this reaction (3 pts.). NBS heat 5. Devise a synthesis of the molecule shown in the box from cyclohexane (3 pts.). 6. Rank the hydrogens by increasing ease of abstraction in a free radical halogenation reaction (2 pts).
Type or paste question here Please provide a structure for each of the following names. 3-Ethyl-2-pentene 1-Bromo-3-methylcyclohexene cis-3-Octene (Z)-3-Methyl-2-hexene Vinylcycloheptane (Z)-1,3,5-Tribromo-2-pentene 1,2-Diethyl-cyclopentene Vinybromide 2,3-Dimethyl-2-butene 3,7,7-Trimethyl-4-octene 4-Isopropyl-1-nonene (E)-3-Methyl-2-heptene
1)- Give the correct names for the structures drawn (i.e. A-E) or draw the structure for each of the names given (i.e.. T) for the compounds below, and use the cis/trans, R/S labeling when appropriate. E T D F 1a-Bromo-2-(trans) Chloro-4-(trans) Ethyl-3-(trans) Methyl-6-(Cis) 2-Hydroxypropyl-5-(trans)- (n-Propyl) Cyclohexane. Note, all of the groups orientations are in reference to la-Bromo Group all of the conformers specifications (e.g., axi the chair conformers of 1)- Give the correct names for the structures drawn (i.e. A-E)...