I consider both substituent are Meryl group
1,2dimetylcycloheaxane
R1 is axial position and R2 also axial position
It is most stable form which is chair form
I
ball & stick + labels Name the above compound, identify each substitutent as axial or equatorial,...
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...
The cyclohexane derivative shown exists primarily in the more stable of the two available chair conformations. Give the position, axial or equatorial, of each of the three groups shown in the more stable chair conformation. If a group divides its time equally between axial and equatorial positions, indicate this with ax/eq The table of "Axial Strain Energies for Monosubstituted Cyclohexanes" found in the "Strain Energy Increments" section of the Reference tool is useful for answering this question. CH-CH2 CI Group...
Is it axial, equatorial, or ax/eq? The cyclohexane derivative shown exists primarily in the more stable of the two available chair conformations. Give the position, axial or equatorial, of each of the three groups shown in the more stable chair conformation. If a group divides its time equally between axial and equatorial positions, indicate this with ax/eq. The table of "Axial Strain Energies for Monosubstituted Cyclohexanes" found in the "Strain Energy Increments" section of the Reference tool is useful for...
The cyclohexane derivative shown exists primarily in the more stable of the two available chair conformations. Give the position, axial or equatorial, of each of the three groups shown in the more stable chair conformation. If a group divides its time equally between axial and equatorial positions, indicate this with ax/eq. The table of "Axial Strain Energies for Monosubstituted Cyclohexanes" found in the "Strain Energy Increments" section of the Reference tool is useful for answering this question. The choices are...
Name the following alkene. ball & stick + labels (Include E/Z designations in your names if appropriate. Omit customary italics.) 2,4-dimethyl-3-heptene
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...
The cyclohexane derivative shown exists primarily in the more stable of the two available chair conformations. Give the position, axial or equatorial, of each of the three groups shown in the more stable chair conformation. If a group divides its time equally between axial and equatorial positions, indicate this with ax/eq. The table of "Axial Strain Energies for Monosubstituted Cyclohexanes" found in the "Strain Energy Increments" section of the Reference tool is useful for answering this question. СІ bCH2CH3 Group...
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
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: