What notation is applicable in this structure? HC CH3 a trans Ob.Z Oc. E d. cis

Question

Question

Answer 1

Answer #1

CH3 CH2CH3 Br i-ethyle-2- Bromo - 1,2-dimethyl-herene groups on the same side. d) cis because 2-methyl

Answer 2

Similar Homework Help Questions

A. 1-cis, 2-cis B. 1-cis, 2=trans C. 1=trans, 2-cis D. 1: Enter Your Answer: OA OB...

A. 1-cis, 2-cis B. 1-cis, 2=trans C. 1=trans, 2-cis D. 1: Enter Your Answer: OA OB OC OD A Correct Draw the major product of the following reaction. Question 9 Br L -CH3 we 3-chs H3C CH3 Create OscerSketch Answer 9 Not Submitted Draw the major product of the following reaction. Question 10 H3CH HO CH3 Create OscerSketch Answer 10 Not Submitted Save Answers 8 Submissions Left
2.1. Name the following compound. Specify cis/trans geometry, if applicable. Q.2. Draw line structure for cis-4-methyl-2-hexene....

2.1. Name the following compound. Specify cis/trans geometry, if applicable. Q.2. Draw line structure for cis-4-methyl-2-hexene. 03. Draw a strucrure with molecular formula CH,20 which exhibits cis/trans isomerism, and also has a chiral center. How many stereoisomers are possible for this molecular formular? Q.4. What is the index of hydrogen deficiency of a compound with molecular formula C-H, BINO? Q.5. How many stereoisomers of 4-chloro-2-pentene exist? a 1 6 . 2 c. 3 d. 4.
3.6: Which of the following compounds can exist as cis–trans isomers? Draw each cis–trans pair. ...

3.6: Which of the following compounds can exist as cis–trans isomers? Draw each cis–trans pair. (a) CH3CH=CH2 (b) (CH3)2C=CHCH3 (c) ClCH=CHCl (d) CH3CH2CH=CHCH3 (e) CH3CH2CH=C(Br)CH3 (f) 3-Methylhept-3-ene The answer is c, d, e ,f but I'm not sure how it works

23) For which of the following alkenes will cis- and trans- isomers not exist? CH3 H₃ C C H₂C CH3 H3CH2C-CH3 Hac нс...

23) For which of the following alkenes will cis- and trans- isomers not exist? CH3 H₃ C C H₂C CH3 H3CH2C-CH3 Hac нсінсін сня сі" A) a) only (B) only C) both a) and c) D) d) only E) both c) and d)
Including the cis or trans designation, what is the IUPAC name of the following substance? It...

Including the cis or trans designation, what is the IUPAC name of the following substance? It is not necessary to put cis or trans in italics. CH3 CH3 CHCH3 H CH3 Submit Answer Retry Entire Group 9 more group attempts remaining Use the References to access important values if needed for this question Including the cis or trans designation, what is the IUPAC name of the following substance? It is not necessary to put cis or trans in italics. Submit...
Including the cis or trans designation, what is the IUPAC name of the following substance? It...

Including the cis or trans designation, what is the IUPAC name of the following substance? It is not necessary to put cis or trans in italics. CH3CH2 Н. CH3 CH3

c. cis-1-metbylbicylol0.4.4ldecan 24. Which structure is syn? d. trans-1-methylbicyclo[0.4.41derane e. not a.-d с. e. not a.-d...

c. cis-1-metbylbicylol0.4.4ldecan 24. Which structure is syn? d. trans-1-methylbicyclo[0.4.41derane e. not a.-d с. e. not a.-d 25. Monocyclic alkenes (for example, cyclepropene, cyclobutene, etc.) up to 7 carbons are all? a. b. R C. S d. Z e. not a.-d. 26. The following stereoisomer of a controlled substance is? (Hint: The alcohol is the 1 carbon.) a. 1R, 2R) b. (1R, 25) c. (1S, 2R) d. (1S, 2S) e. not a.-d 27. The carbon with the asterisk is? a. с....
What is the correct IUPAC name for the compound shown below? CH3 HC С=С H CH2CH3...

What is the correct IUPAC name for the compound shown below? CH3 HC С=С H CH2CH3 O (E)-3-methyl-2-pentene O trans-3-methyl-3-pentene O cis-2-ethyl-2-butene O (Z)-2-ethyl-2-butene O (Z)-3-methyl-2-pentene
5. Name the following alkene molecules. Be sure to include cis/trans designations whenever necessary! CH3 CH3...

5. Name the following alkene molecules. Be sure to include cis/trans designations whenever necessary! CH3 CH3 Br CI

REferences Name the following cycloalkane. labels ball & stick (Use cis/trans terms if applicable. It is...

REferences Name the following cycloalkane. labels ball & stick (Use cis/trans terms if applicable. It is not necessary to use italics in writing compound names.) The IUPAC name is: