The structure of given name is
Draw the structures for the following compounds: (3Z,5Z)-2-chloro-4,5-diethyl-3,5-nonadiene PLEASE EXPLAIN! (3 points) Draw the structures for...
Draw the structures for the following compounds: (3Z,5Z)-2-chloro-4,5-diethyl-3,5-nonadiene
1. Draw line-angle structures for the following compounds: a) (20,4E)-1-chloro-3-methyl-2,4-hexadiene b) (32,5E)-4-methyl-3,5-nonadiene c) (32,5Z)-4,5-dimethyl-3,5-nonadiene d) (35,5E)-2,5-dibromo-3,5-octadiene
lculate the degrees of unsaturation in the following compounds. a. C12H16N302Br b. C8H10C14 c. C9H20N4 d. C15H18 4. Draw structures for the following hydrocarbons. a. 3,5-diethyl-4-isopropyl-2,6-octadiene b. 4,5-dimethyl-1,4,7-decatriene c. 1-chloro-3-bromo-3-heptene d. 2-methyl-1,3-cyclopentadiene e. 4-isopropylcyclohexene
Draw structures for the following compounds. a. 2-chloro-1,3-cyclopentadiene b. 2-bromo-5-nitroaniline c. 2-chloro-5-fluoro-3-octyne
1. 3-methyl-1-butene on reaction with H-Cl forms two products, namely 2-chloro-3- methylbutane (minor) and 2-chloro-2-methylbutane (major). Illustrate the mechanism for the formation of these two products. Use curved arrows to illustrate electron movement and all intermediates must be shown. 2. 3,3-dimethyl-1-butene on reaction with HBr forms two products, namely 3-bromo-2,2- dimethylbutane (minor) and 2-bromo-2,3-dimethylbutane (major). Illustrate the mechanism for the formation of these two products. Use curved arrows to illustrate electron movement and all intermediates must be shown. 3. Calculate...
Draw the structures of the two possible products- 3-chloro-1-butene and 1-chloro-2butene. Explain the type of isomers of the two compounds.
9. (10 pts) Draw structures for the following compounds: (a) (2S,4S)-2-Bromo-4,5-diethylheptane (b)(R)-3-hexyn-2-ol
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. (4 pts) Draw the structures of the two possible products- 3-chloro-1-butene and 1-chloro-2- butene. What type of isomers are these two compounds?
Draw the structures for the following compounds. a) (3Z,5S)-4-bromo-5-chloro-2-methylhexa-1,3-diene b) (5S,7S)-5-(bromomethyl)-7-chloro-oct-2-yne c) (1S,5S,6S)-6-bromo-5-[(1R)-1-chloroethyl]cyclohex-3-enol d) 2-bromo-4-[(1R)-1-hydroxyethyl]benzoic acid e) (3S,4S,5S)-5-amino-3-hydroxy-4-methylhexanal f) (Z,2R,4R)-6-bromo-4-chloro-N-ethyl-N-methylhept-5-en-2-amine g) [(1S)-1-chloroethyl] (Z,3R)-5-chloro-3-methoxyhex-4-enoate h) (Z,3R)-3-bromo-4-chloro-7-methyloct-4-enoic acid i) (3S)-6-bromo-N-ethyl-N,3-dimethylhex-4-ynamide j) (Z,3R,4S)-6-bromo-3-[(1S)-1-chloroethyl]-4-hydroxyhept-5-en-2-one