Question

Draw the structure of the following: A) 5- butyl- 2,3,4- trithyldecane B) 5,5,6-trimethyl-1-heptene C) 3,3-diethyl-trans-4-nonene

Draw the structure of the following:
A) 5- butyl- 2,3,4- trithyldecane
B) 5,5,6-trimethyl-1-heptene
C) 3,3-diethyl-trans-4-nonene

Homework Answers

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
List the following molecules in order of increasing heat of combustion and explain why. A: 2,3,4-trimethyl-1,3-pentadiene...
List the following molecules in order of increasing heat of combustion and explain why. A: 2,3,4-trimethyl-1,3-pentadiene B: 2-isopropyl-1,4-pentadiene C: 3,3-dimethyl-1,5-hexadiene D: 4,5-dimethylcyclohexene
Answer the following questions for this organic compounds: 1-Hexine, Methanal, 3,3-dimethyl-1-heptene, and Chloropropane. 2 inminent properties...
Answer the following questions for this organic compounds: 1-Hexine, Methanal, 3,3-dimethyl-1-heptene, and Chloropropane. 2 inminent properties for each 3 industrial uses for each water solubility of each (C0)
Draw the structure that corresponds to the following names R-2-bromobutane (E)-3-methyl-2-pentene 3,3-dimethyl-1-hexyne
Draw the structure that corresponds to the following names R-2-bromobutane (E)-3-methyl-2-pentene 3,3-dimethyl-1-hexyne
10. View the first compound name provided in Table 6. Follow the steps below and draw...
10. View the first compound name provided in Table 6. Follow the steps below and draw each part of the structure on a piece of paper. a. Determine the number of carbons present in the compound based on the base name. b. Draw the carbon chain and include any double or triple bonds if indicated in the suffix of the base name. c. Number each carbon. The carbons can be numbered from left to right or right to left. d....
Which of the following is not a valid IUPAC name?           (a) cis-1-bromo-5-chloro-2-hexene   (c) 1,8-difluoro-3-methyloctane           
Which of the following is not a valid IUPAC name?           (a) cis-1-bromo-5-chloro-2-hexene   (c) 1,8-difluoro-3-methyloctane           (b) 6-chloro-1-heptene                      (d) These are all fine. Which molecule is chiral?            (a) 3,3-diethylheptane                      (c) 2-propylcyclopentanone            (b) 1,1-difluorocyclodecane              (d) none of these
1. Draw the line-bond structure for stearic acid and linoleic acid. Identify which fatty acid is...
1. Draw the line-bond structure for stearic acid and linoleic acid. Identify which fatty acid is saturated and which is unsaturated. 2. Trans fats are produced during the hydrogenation of polyunsaturated oils.             a. What is the typical configuration (cis or trans) about the double bond of a monounsaturated fatty acid? b. Draw the structure of cis-palmitoleic acid. c. Draw the structure of trans-palmitoleic acid. d. Why are trans-fatty acids considered to be a health hazard? e. Is it better...
Draw the two flip chair conformations of trans 1-ethyl-4-methylcyclohexane. Also, draw a Newman projection of the...
Draw the two flip chair conformations of trans 1-ethyl-4-methylcyclohexane. Also, draw a Newman projection of the less stable conformation (cite along C1-C2 and C5-C4)
Draw the structures for the following two compounds, using wedges and dashes: a) cis-1,3-dimethylcyclobutane b) trans-1-ethyl-2-methylcyclopentane....
Draw the structures for the following two compounds, using wedges and dashes: a) cis-1,3-dimethylcyclobutane b) trans-1-ethyl-2-methylcyclopentane. For cis-1,3-diethylcyclobutane draw a) a stereoisomer and b) a constitutional isomer.
Alcohol Nomenclature: Draw a structural formula for the following - show stereochemistry only if given in...
Alcohol Nomenclature: Draw a structural formula for the following - show stereochemistry only if given in the name, if group is achiral and do not use wedged or hashed bonds on it. a. trans-2-chlorocyclopentanol b. 3,3-dimethylcyclohexanol c. 2,3-dimethyl-2-hexanol
1. For the preparation of 2-bromo-4-n-butyl phenol from phenol, the first step is: A. acylation B....
1. For the preparation of 2-bromo-4-n-butyl phenol from phenol, the first step is: A. acylation B. conversion to anisole C. HNO3 / N2SO4 * And if able to answer: 2. The n-butyl group is installed by:
ADVERTISEMENT
Need Online Homework Help?

Get Answers For Free
Most questions answered within 1 hours.

Ask a Question
ADVERTISEMENT