18. (15 pts) Nomenclature: Provide the systematic IUPAC name for each of the following molecules. Indicate...
12. (5 pts) Nomenclature: Provide the systematic IUPAC name for each of the following molecules. Indicate stereochemistry if applicable (R,S). CI
11-14 please Provide the systematic IUPAC name for each of the following compounds. Indicate RIS configurations of any stereocenters (excluding Problem-I), as well as absolute (E/Z) configurations iT applicable. For the first two molecules, draw the Newman projection about the indicated carbon bonds (--) Excluding Problem 11.) он 12.) Br 13.) 14) н.с Provide the systematic IUPAC name for each of the following compounds. Indicate RIS configurations of any stereocenters (excluding Problem-I), as well as absolute (E/Z) configurations iT applicable....
3. Name each of the following compounds using IUPAC nomenclature, including stereochemistry if applicable. (18 points) Br, I "I н "Br
Give the IUPAC name for this compound. Please note that your answer may not contain any typographical errors or incorrect punctuation. Give the IUPAC name for this compound. Please note that your answer may not contain any typographical errors or incorrect punctuation. CI Give the IUPAC name for this compound. Please note that your answer may not contain any typographical errors or incorrect punctuation. Cis-trans isomerism is also possible in molecules with rings. Draw the cis and trans isomers of...
POSTLAB QUESTIONS Name Date Instructor Organic Models and Nomenclature 1. Name the following compounds using the IUPAC nomenclature system: a. CH CH.CH,CH,CH, Peptone b. CH CH CHCHCH, I methu Pentare CH, CH, c. CH CH CCH CH 2. Draw the constitutional (structural) isomers of C,H, 3. Draw the structure of trans-2-butene, and then sketch the product that would result if this compound reacted with bromine, Br, Postlab Questions: Organic Models and Nomencla 4. Circle the functional groups on the molecules...
Provide the systematic name for each of the following isomeric amides with the chemical formula C6H1NO (Be sure to indicate double bond stereochemistry using (E) (Z) notation. Indicate stereochemistry in rings with the terms cis or trans. It is not necessary to use italics in writing compound names.) ball & sticklabels ball & sticklabels ball & sticklabels
2). Give the systematic (IUPAC) names of the following alkenes. a. CH2=CH-CH2-CH=CH23. Determine which compounds show cis-trans isomerism. Draw and label the isomers, using both the cis-trans and E-Z nomenclatures where applicable. a. pent-1-ene b. pent-2-ene c. hex-3-ene d. 1,1-dibromopropene e. 1,2-dibromopropene
Provide the systematic name for each of the following isomeric amides with the chemical formula C6H11 NO. (Be sure to indicate double bond stereochemistry using (E) (Z) notation. Indicate stereochemistry in rings with the terms cis or trans. It is not necessary to use italics in writing compound names.) ball & stick - + labels ball & stick - + labels ball & stick - + labels
1. (4 pts) On the line drawn below, provide the systematic (IUPAC) name for the following structure. Be sure to include stereochemistry when necessary. Show all work for full credit.
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