Name the alkene(s) with the molecular formula C6H12 that have a single methyl branch and that show E/Z isomerism. Use E/Z to describe stereochemistry around the double bond as appropriate. Do not use cis/trans. If there are fewer than 4 possible isomers, leave the appropriate number of spaces blank.
Name the alkene(s) with the molecular formula C6H12 that have a single methyl branch and that...
Draw the structure(s) of the alkene(s) with the molecular formula C6H12 that have a single methyl branch and that show E/Z isomerism.
6. Draw and name all the alkene cis-trans isomers corresponding to the molecular formula C5H10. (Hint: there are only two.)
1.Draw the structure(s) of all of the alkene isomers, C6H12, that contain a methylene group. 2.Name all of the alkene isomers, C6H12, that contain an unbranched chain and that have E/Z isomers.
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
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
There are several aromatic compounds with the formula CgH9Cl. Name those that have a trisubstituted ring where the methyl groups are oriented meta. If you choose to use ortho, meta, or para in your name, abbreviate these prefixes with o, m, or p. If there are not 3 isomers that fit the description, leave the appropriate number of spaces blank. Isomer #1: Isomer #2: Isomer #3:
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
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Part A: Molecular Modeling 1. Models of 1,2-Dibromoethene Br, H Br Br C= C H Br trans-1, 2-dibromeoethene cis-1, 2-dibromoethene A (trans) B (cis) Figure 7.2. Geometric Isomers. Procedure Part A Construct a model of 1,2-dibromoethene (CHBr=CHBr) so that if viewed from above and in front, see Figure 7.2. Answer all questions on report sheet. 1. Are the models superimposable? 2. Are A and B stereoisomers? Are they enantiomers or diastereomers? 3. Name A, use the E-Z system. 4....
Chapter 11: 1. What is a prime rule in naming alkenes? a. Find the longest carbon chain. b.Find the longest carbon chain containing the alkene. c. Find whether the alkene has a cis- or trans- configuration. d.Find how far the alkene functionality is from either end. 2. What is the IUPAC name of the following alkene? a. cis-5-methyl-2-heptene b. trans-2-ethyl-4-hexene c. trans-5-methyl-2-heptene d. trans-3-methyl-5-heptene 3. What is the hybridization, geometry, and bond angle of the carbon marked by an asterisk?...
(c). When compound A reacts with NaoMe, a single chiral alkene F with the molecular formula of CH14 is formed. Draw the structure of alkene F in the box below (show appropriate stereochemistry), and circle the mechanism for the transformation of Ato F. (3 + 2 pts) F Me „Me NaoMe A Sn2 Sn1 E2 E1 (d). When compound A is reacted with potassium methylthiolate (KSMe) in acetone, a single chiral compound G with the molecular formula of CH18S is...