Question

B) water concentrated acid A) water dilute acid D) hydroboration-oxidation C) oxymercuration demercuration 13. An unknown compound was treated with Os followed by work-up with dimethylsulfide and the following products were identified. From the information provided what is the most likely structure for this unknown compound. Part 2: Nomenclature (6 Points) For each of the following, name or draw the structures according to luPAC nomenclature rules, including stereochem when necessary. OH
Please provide nomenclature for bottom problem

0 0
Add a comment Improve this question Transcribed image text
Answer #1

Longest carbon chain is 6 carbons. So parent alkane is hexane Double bond should get less number so starting from double bond

Add a comment
Know the answer?
Add Answer to:
Please provide nomenclature for bottom problem An unknown compound was treated with O_3 followed by work-up...
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. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • 8.1) 8.5) Give the appropriate IUPAC name for the following structural formula of a halogenated compound....

    8.1) 8.5) Give the appropriate IUPAC name for the following structural formula of a halogenated compound. CH3 CI Нас (Where stereochemistry is shown, include a designation of configuration in your answer. Use cis/trans designations only to represent stereochemistry for cyclic compounds. It is not necessary to use italics in writing compound names.) Name: There are five cycloalkanes with the molecular formula C5H10. When treated with chlorine at 300°C, isomer A gives one monochlorination product. Under the same conditions, isomer B...

  • Please answer all parts for good rating! A) Name the following compounds using IUPAC rules: B)...

    Please answer all parts for good rating! A) Name the following compounds using IUPAC rules: B) Provide the structures for the compounds below: 4-bromobutanal acetophenone yy fty For the following reaction, provide the structure of the open- chain form of the compound (pay attention to stereochemistry) and the complete arrow-pushing mechanism for the reaction. open-chain form HO Starting with the compound shown and only alcohols (including diols) of three carbons or less, suggest a means by which to achieve the...

  • 1. (2 points) Provide the IUPAC name for the following structure. он 2. (2 points) Draw...

    1. (2 points) Provide the IUPAC name for the following structure. он 2. (2 points) Draw the structure from the provided name: 5-chloro-2,2-dimethylcyclohexane-1,3-dione. 3. (6 points) The following reaction produces five different substitution and elimination products, (a) Draw these products and (b) rank the stability of the elimination products by using the labels (E1-E3) according to the products as you have entered them. substitution product S1 substitution product S2 HzC04 CF, H-OH elimination product E1 elimination product E2 elimination product...

  • need help on the last hw problems please explain and answer 43. An unknown compound of...

    need help on the last hw problems please explain and answer 43. An unknown compound of formula CeH16 was found to be optically active. On catalytic reduction of the unknown compound over a palladium catalyst, 2 equivalents of hydrogen were absorbed. Ozonolysis of the unknown compound gave two products: one was identified as an optically active dialdehyde of formula CsHaO2; the other compound was identified as acetaldehyde (CH3CHO). The most likely structure of the unknown compound is B. CH.CH-CH-CHECH CH...

  • Please take your time to answer all questions clearly and correctly... More Nomenclature and Symmetry Learning...

    Please take your time to answer all questions clearly and correctly... More Nomenclature and Symmetry Learning Objectives: 1, Determine the rules for naming coordination compounds including special orientation of ligands 2. Use the rules to determine structures and formula from names and vice versa. 1. Isomerism in metal complex nomenclature: For the remainder of this assignment you can reference Figure 1 which contains a collection of metal complex structures with their chemical names and chemical compositions. Answer questions a -e....

  • 1. Provide a systematic IUPAC name for the compound, including R/S and E/Z if appropriate. (3...

    1. Provide a systematic IUPAC name for the compound, including R/S and E/Z if appropriate. (3 pts.) 2. Draw the bond-line structure of (2,4Z)-2,5-dibromo-3-methylhexa-2,4-diene. (3 pts.) 3. Label the most stable and the least stable alkene (4 pts.) 4. Consider the substitution reaction below. (4 pts.) NaSH DMF SH in why this reaction proceeds through an SN mechanism and not an S2 mechanism a) Explain why this reaction proces o b) Explain why this reaction produces a racemic mixture of...

  • Key concepts: molecular represenations, stereolsomers, RS enantiomeric excess, IPAC naming covention Provide the IUPAC name for...

    Key concepts: molecular represenations, stereolsomers, RS enantiomeric excess, IPAC naming covention Provide the IUPAC name for each of the following molecules 0% HJC BM How similar are the names for B and C, even though there is the single change to the structure 2 Rank the priorities of these functional groups and substituents using Cahn-Ingold-Prelog nomenclature. Highest priority will be 1 and lowest will be 5; show your rationale CH:CH:CH CH CHCH:CH CHs,-SCH,-CH: CH:CH:CHCH CHCH, -CH2NHOH,-CH:NO Draw dash/wedge representations for...

  • (C) Protonation of alkene to form a carbocation followed by addition of bromide ion (D) Addition...

    (C) Protonation of alkene to form a carbocation followed by addition of bromide ion (D) Addition of the proton to one face of the alkene with simultaneous delivery of a bromide ion from a different molecule of H-Br. 11. Which compound is the strongest nmucleophile for reaction of methane methanesulfonate (CHOS0.CH) in methanol at room temperature? (You may assume that everything is soluble in methanol) (A) potassium bromide (B) cesium iodide (C) sodiam chloride (D) lithium flaoride 12. Which proton...

  • 6 In Part C, which of the anta heartburn? Use the information you o which of the antacids you tested would b...

    6 In Part C, which of the anta heartburn? Use the information you o which of the antacids you tested would be the most effective at neutralizing stomach acid to w a offerences in the effectiveness of the antacids you tested e the information you obtained from the antacid package labels to offer an explanation for the some antacids produce bubbles when they react with acids. The bubbles are carbon dioxide (CO) released by decomposition of carbonic acid (H.CO) produced...

  • Experiment Write Up Proposal You will write up a synthesis procedure for one reaction that could...

    Experiment Write Up Proposal You will write up a synthesis procedure for one reaction that could be potentially run in a face- to-face Chem 2321 lab session. Your proposal will include an introduction and procedure. The procedure will include step-by-step instructions for running the reaction (including reaction monitoring), work-up. (product isolation and purification), and analysis (characterization). You will need to include sample calculations for percent yield and provide sample spectra analysis. You must upload your proposal as a single document...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT