1. Give IUPAC names for the following compounds: (a) H3C CH3 (b) CH3 H2C=CHCHCCH3 CH3CH2CH=ĊCH2CH3 CH3 (d) CH3 CH3 (c) CH(CH3)2 CH3CH2CC=CCHCH3 CH3 2. Which of the following compounds can exist as cis-trans isomers? Draw each cis-trans pair. (a) CH3CH=CH2 (c) CICH=CHCI (е) СH3СH2CH—С(Br)CHҙ (b) (CH3)2С—СНCHЗ (d) CH3CH2CH=CHCH3 (f) 3-Methylhept-3-ene

1. Give IUPAC names for the following compounds: (a) H3C CH3 (b) CH3 H2C=CHCHCCH3 CH3CH2CH=ĊCH2CH3 CH3 (d) CH3 CH3 (c) CH(CH3)2 CH3CH2CC=CCHCH3 CH3 2. Which of the following compounds can exist as cis-trans isomers? Draw each cis-trans pair. (a) CH3CH=CH2 (c) CICH=CHCI (е) СH3СH2CH—С(Br)CHҙ (b) (CH3)2С—СНCHЗ (d) CH3CH2CH=CHCH3 (f) 3-Methylhept-3-ene

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter4: Organic Compounds: Cycloalkanes And Their Stereochemistry

Section4.SE: Something Extra

Problem 35AP: A 1, 2-cis disubstituted cyclohexane, such as cis-1, 2-dichlorocyclohexane, must have one group...

See similar textbooks

Similar questions

Citing down the C3-C4 bond, and using the drawings below, complete the Newman projections for all staggered and eclipsed conformations of hexane. Which staggered conformation has the lowest energy? Which eclipsed conformation has the highest energy?
5. Draw all the structures of constitutional isomers with the molecular formula:a) C4H6b) C4H9Brc) C4H10O
1. (A) DRAW are all the possible isomers for dibromobutane and the cylic isomers for C3H4Br2 (B) WRITE THE STRUCTURAL OR CONDENSED FORMULAR FOR C3H7Br C3H6Br2 C3H5Br3 C5H11Br
Is the geometry of CH2BrCl, the same as CH3Cl and CH4? Briefly explain the evidence for your answer
a. For each disubstituted cyclohexane below, draw its ring-flip isomer. Circle the most stable conformation and label the substituent groups as axial or equatorial. ( see image) b.Draw and name the seven constitutional isomers (all contain a ring of some size) for cycloalkane, C6H12.
Draw 3-D structures for all possible constitutional isomer and Write IUPAC names and include cis-trans a) )(Only three-membered rings) C3H6, C3H5CL, and C3H4CL2 b)(Only five-membered rings) C5H10, C5H9CL and C5H8CL2
Draw all of the constitutional isomers with molecular formula of C6H12 that possess one pi bond. Don't include cyclic structures.
C5H8Cl2 can you name and draw all isomers , make sure each has a 5 membered cyclic ring . And use E,Z when approp
Draw all possible constitutional isomers for C7H16
1. Tell whether the following pairs of structures are identical or not. 2. For those pairs that are not identical, explain what types of isomers they are. 3. If there are chiral centers, denote them with the correct R,S.
(a) Draw the nine isomers having the formula C7H16 . (Hint: There is one structure with a seven-carbon chain, two structures with six-carbon chains [one is illustrated in the margin above], five structures with a five-carbon chain, and one structure with a fourcarbon chain.)(b) Identify the isomers of C7H16 that are chiral.
Draw and name the following:a. 4 isomers of C10H22 with 5 carbons as the longest chain