Draw two organic molecules (which are not stereoisomers) in the box below that is an open-chain ketone containing 5 carbons and no C-C multiplebonds (You have three chances until the answer will be given; you have already tried 0 times)Draw only one molecule in each drawing box.Compound #1Compound #2

We are tasked to draw a ketone containing 5 carbons and no multiple C-C bonds. An organic compound…

Answered: Draw two organic molecules (which are…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter6: Alkanes & Alkenes

Section: Chapter Questions

Problem 21E

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Draw two organic molecules (which are not stereoisomers) in the box below that is an open-chain alcohol containing 4 carbons and C-C one triple bond (You have three chances until the answer will be given; you have already tried 0 times) Draw only one molecule in each drawing box. Compound #1 Compound #2
Draw two organic molecules (which are not stereoisomers) in the box below that is an open-chain amide containing 3 carbons and no C-C multiple bonds (You have three chances until the answer will be given; you have already tried 0 times) Draw only one molecule in cach drawing box. Compound #1 Compound #2
Draw two organic molecules in the box below that are chain isomers of the following molecule and are still methyl esters (You have two chances until the answer will be given; you have already tried 0 times) Chain isomers have the same functional group but a different connectivity of the carbon backbone H₂C || H₂ C_H_C CH 3 CH3 Draw only one molecule in each drawing box. Compound #1 Compound #2
2) In the space below, draw all of the stereoisomers of molecule a. a) CH 3 H-C-F H-C-F F-C-H CH3
Shown are two stereo representations of lactic acid. Compare the two structures shown. Determine whether they represent identical molecules or mirror images. identical COOH COOH H" OH CH3 H3C HO Determine the absolute configuration of the two structures. Left: S✔ Right: S An error has been detected in your answer. Check for typos, miscalculations etc. before submitting your answer. H
Only typed solution
Draw the cis form of the only compound that has stereochemistry: CH3 CH3 CH 3 Draw the trans form of the only compound that has stereochemistry: Edit ||||CH 3 Edit Your answer is partially correct. Try again. Name the molecule whose longest chain has five carbons: (Do not add any spaces between any terms) cyclopentane Name the molecule whose longest chain has four carbons: (Do not add any spaces between any terms) methylcyclobutane Name the molecule which has a two-carbon long chain substituent: (Do not add any spaces between any terms) Tethylcyclopropane Name the molecule that has a quaternary carbon: (Do not add any spaces between any terms) T1,1-dimethylcyclopropan Name the form (cis or trans) of the only compound with stereochemistry: (Do not add any spaces between any terms) (1R, 2S)-1,2-dimethylcyc
Check the pox under each compound that exists as a pair of mirror-image twins. If none of them do, check the none of the above boxunder the table. HO HO HO-CH CH2-CH OH НО — НО HO CH2 CH-CH2 OH Но CH3 Но CH3-C-CH2-C-CH3 CH3 -CH2 C-CH3 Но CH3 CH2 CH-CH2 OH CH3 НО none of the above Explanation Check O 2022 McGraw Hill LLC. All Rights Reserved. Terms of Use Privacy Center Ac Delete F7 レレゴ

Within the drawing area below, draw the structure of two separate constitutional isomers that have the molecular formula C_H and contain one ring. 7 14 Within the drawing area below, draw the structure of two separate constitutional isomers that have the molecular formula C-H14 and contain one ring.
Draw 2 sets of molecules. The first set should be constitutional isomers. The second set should not be constitutional isomers. Explain why the first set of isomers is constitutional and why the second set is not.
circle the molecules below which you would expect to be extra stable, and draw a box around any molecules which you would expect to be particularly unstable. Assume molecules are planar, and do not focus on angle strain issues (that is, are the first two molecules more or less stable than other 3-membered rings with one C=C double bond?). NH NH The last molecule has an IR spectrum which does not match the structure drawn. Specifically, it does not possess a strong carbonyl absorption anywhere near 1700 cm-. What does this tell you about the actual structure of the molecule? Draw the mechanism for a reaction, catalyzed by basic water, by which it forms a constitutional isomer, and explain why this isomerization reaction is both rapid and exothermic. H НО H,O Do you expect a similar rapid, exothermic isomerization for the second-to-last molecule (the 4-membered amide)? Why or why not? Draw the structure of the analogous isomer.
OH Check the box under each structure in the table that is an enantiomer of the molecule shown below. If none of them are, check the none of the above box under the table. m H Br Molecule 1 Molecule 2 Molecule 3 Х Br OH H CI Br OH HO יייון CI H Br ་་་་་ H Molecule 4 Molecule 5 Molecule 6 H OH Br HO "ייון Br H .au G\ CI OH Br H none of the above U

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