Name the following alkene. ball & stick + labels (Include E/Z designations in your names if...
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
Name all of the branched alkene isomers, CH12, that contain 2 methyl branches. pt Include E/Z designations in your names if appropriate. Omit customary italics. If there are fewer than 4 possible compounds, leave the appropriate number of fields blank. Isomer 1: 2,3,-dimethyl-2-butene Isomer 2: 2,3-dimethyl-1-butene Isomer 3: 3,3-dimethyl-1-butene Isomer 4: pt pt pt pt pt
Relerences Provide an IUPAC name for the compound below. ball & stick + labels (Specify (E) or (Z) stereochemistry, irrelevant for straight chain alkenes only. It is not necessary to use italics in writing compe names. Pay attention to commas, dashes, and parentheses.) Submit Answer Retry Entire Group TReview TOPICS (References Provide an IUPAC name for the compound below. ball & stick + labels (Specify (E) or (Z) stereochemistry, if relevant for straight chain alkenes only. It is not necessary...
Provide an IUPAC name for the compound below. ball & stick - + labels (Specify (E) or (Z) stereochemistry, if relevant, for straight chain alkenes only. I use italics in writing compound names. Pay attention to commas, dashes, and pa
Give an TUPAC name for the substances below: ball & stick labels ball & stick labels (Abbreviate ortho (o), meta (m), and para (p), if you use these terms. It is not necessary to use italics in writing compound names.) 1st structure: 2nd structure
ball & stick + labels Wame the above compound, identify each substitutent as axial or e table or less stable form. • Omit customary italics from your name. Substitutents R1 and R2 are designated in the order they a increments are available in the table below. Cote Reference • Omit customary italics from your name. • Substitutents R1 and R2 are designated in the order they appear i increments are available in the table below. 1. The IUPAC name is...
ball & stick + labels Name the above compound, identify each substitutent as axial or equatorial, and tell whether the conformation shown is the more stable or less stable form Omit customary italics from your name. • Substitutents R1 and R2 are designated in the order they appear in the IUPAC name. Axial/oquatorial strain energy increments are available in the table below. 1. The IUPAC name is 2. Position of RI Position of R2 3. The conformation shown is the...
REferences Name the following cycloalkane. labels ball & stick (Use cis/trans terms if applicable. It is not necessary to use italics in writing compound names.) The IUPAC name is:
Provide an IUPAC name for the structure shown. ball & stick - + labels (Use cis/trans terms for cyclic structures. Do not specify stereochemistry in other cases. It is not necessary to use italics in writing compound names.) Name: Submit Answer Retry Entire Group 6 more group attempts remaining Provide an IUPAC name for the structure shown. ball & stick + labels (Use cis/trans terms for cyclic structures. Do not specify stereochemistry in other cases. It is not necessary to...
Name the following cycloalkane. ball & stick - + labels (Use cis/trans terms if applicable. It is not necessary to use italics in writing compound names.) The IUPAC name is: Submit Answer Try Another Version 9 item attempts remaining