Name the following compounds C. Cis-1-iodo-4-1-methylethyl)cyclohexane o ECM @ $$ VID
I CHE cis-1-iodo-1-propene trans-1-iodo-1-propene Match the phrases in the left column to the appropriate blanks in the sentences on the right. Make certain each sentence is complete before submitting your answer. ► View Available Hint(s) 1. Try to manipulate the cis and trans isomers of 1-iodo-1-propene by chiral with superimposable mirror images rotating bonds, but without breaking bonds. The two structures are diastereomers (stereoisomers that are not superimposable mirror images) 2. Starting with cis-1-iodo-1-propene add two bromine atom across the...
2. Name or draw (as appropriate for the following compounds: OH 1701111 B. (1R)-1-(1-methylethyl)-4-propoxycyclohex-3-en-ol D. (1R, 32, 55, 6E, 95)-5-ethyl-9(N,N-diethylamino)cyclodec-3,6-dien-1-ol ol بما
1. Draw the structures of: a) (Z) 2-iodo-3-methyl-2-heptene b) cis non-3-en-5 yne Give the IUPAC name of the following compounds, including steochemistry. a) F CH2CH2Br CH3CE 2. a) Draw the most stable chair conformation of cis 1,3-difluorocyclohexane. b) Draw a Newman projection of 2-iodo-3-methylpentane looking down the 3. Compound X has the formula CoHB2Br4. Compound X reacts with excess H2/Pd to give CATHa6Bra. How many does compound X have? Show how you got your answer. rings 4. For each pair...
4. Name the following compounds and state the orientation around the double bond (cis/trans or E/Z) (10 pts)
4. Name the following compounds and state the orientation around the double bond (cis/trans or E/Z) (10 pts)
Give the IUPAC name for each of the following compounds. Include R/S or cis/trans designation at the stereogenic center(s) in the name. CHE CH, O Brº on CH₃ IsoTCH Name: (35,75,95) - 3- bromo - 1 CH₂ CH3 **use cis/trans ONLY** Name: lution of an enantiomerically pure sample of (R)- 3-chloropentanoic acid is made by dissolving 2
Name or draw the following molecules (use cis/trans naming system) 1. Name or draw the following molecules (use cis/trans naming system): CI CI CH3 CH2CH3 a. b. c. 4-ethyl-6-(1,2-dimethylpropyl)decane 2. Draw all of the resonance structures for the following compounds. CH2
1. Write IUPAC name of the following compounds? Include their stereochemistry (E, Z or cis-trans) in their names.
these are the phrase options Part Build models for the two isomers of 1-iodo-1-propene, then complete the sentences that describe these models. CH I CHE cis-1-iodo-1-propene trans-1-iodo-1-propene Match the phrases in the left column to the appropriate blanks in the sentences on the right. Make certain each sentence is complete before submitting your answer. View Available Hint(s) Reset chiral with superimposable mirror images 1. Try to manipulate the cis and trans isomers of 1-iodo-1-propene rotating bonds, but without breaking bonds....
Draw each of the following compounds, including all hydrogens. Both chair forms of cis-3-isopropylcyclohexanol. Circle the one which is more stable. (E)-3-iodo-N-i:opropyl-N-mcthylhcx-2-en-4-yn-1-amine