1. (2E,4Z)-4-methylhepta-2,4-diene
2. Yes, conjugated

1. (3 pts) Name the following alkene. Include stereochemistry designations. 4methyl-2,5hpten 2. (1 pts) Is the...
Name the following alkene. ball & stick + labels (Include E/Z designations in your names if appropriate. Omit customary italics.) 2,4-dimethyl-3-heptene
5. Name the following alkene molecules. Be sure to include cis/trans designations whenever necessary! CH3 CH3 Br CI
name the following alkene. (include E/Z designations in your names
if appropriate. Omit customary italics.)
Draw the product(s) of the reaction of the alkene below with
O3, followed by Zn in acetic acid
please answer both questions.
+labels ball & stick ball & stick labels
1. Name the following compounds using the IUPAC system. No stereochemistry designations needed. a. OH HO b. YY c. d.
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
1. Name the following molecules systematically and include any necessary stereochemistry) (16 pts.): CI. CI
Give the structure or name (whichever is appropriate) for the following. Make sure to include stereochemistry when needed. Read section 10.3 and watch alkene nomenclature video. (E-3-methyl-2-heptene (Z)-1,3,5-tribromo-2-pentene
Name the following alkene. Be sure to indicate stereochemistry and use hyphens (-) notendashes (-).
Name the following alkene. Be sure to indicate stereochemistry and use hyphens (-) not endashes (-). Hocach = C H3C-CH2 CH3
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.