Br 37) Name the following molecule (Hint: check the priority list) A) 7-bromo-4-methyl-5-ene-heptyne B) 4-methyl-7-bromo-5-ene-heptyne C) 1-bromo-4-methyl-6-yne-2-heptene D) 4-methyl-1-bromo-6-yne-2-heptene E) None of above 38) Name the following bicyclichydrocarbon A) bicyclo[4.2.1]nonane B) bicyclo[4.2.1]non-3-ene C) bicyclo[4.2.1]non-4-ene D) bicyclo[1.2.4]nonene

Br 37) Name the following molecule (Hint: check the priority list) A) 7-bromo-4-methyl-5-ene-heptyne B) 4-methyl-7-bromo-5-ene-heptyne C) 1-bromo-4-methyl-6-yne-2-heptene D) 4-methyl-1-bromo-6-yne-2-heptene E) None of above 38) Name the following bicyclichydrocarbon A) bicyclo[4.2.1]nonane B) bicyclo[4.2.1]non-3-ene C) bicyclo[4.2.1]non-4-ene D) bicyclo[1.2.4]nonene

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

ChapterNW1: Nomenclature Worksheet 1: Naming Alkanes & Cycloalkanes

Section: Chapter Questions

Problem 1CTQ

See similar textbooks

Similar questions

Is it option (b)1-bromo-6-chlorocyclohexene?
Which of the structures below is (4R)-4ethyl-2,4- dimethylcyclohexan-1-one?
Please predict the outcome of the addition of HBr to (a) trans-2-pentene, (b) 2-methyl-2-butene, and (c) 4-methylcyclohexene. Also please list how many isomers can be formed in each case? Thank you
4 what is the ftir interpretation of 1-chloro-1-methylcyclohexane?
Your task is to synthesize trans-1, 2-cyclohexanediol, beginning with cyclohexene. What reagent(s) will accomplish this task in good yield? Group of answer choices cold aqueous KMnO4 PCC, CH2C12, 0 oC excess dilute aqueous acid (H2O /H +1) MCPBA followed by dilute aqueous acid (H2O / H+1) Please answer fast i give you upvote.
I put in the answer for compound A, (dimethyl‐lambda4‐sulfanylidene)cyclopropane, and the product 9‐oxadispiro[2.0.44.13]nonane, in the boxes, but it says it's incorrect. What am I not getting?Thank you for your help!
1-ethylcycloheptene + cold, dilute KmnO4
BENZOIC ACID(Screenshot2113) : Find Bonds, Absoprtion Peaks [cm-1] and their functional groups (Alkane/Alyne/Alchol/Arene/etc..)
Does the data provide evidence for the claim that the reaction of Br2 with alkenes proceeds via anti‐addition? The mleting point of the product was found to be 234.5-235.5C chemical reaction: trans-stilbene+pyrimindine tribromide --->acetic acid 1,2-di bromo-1,2-diphenylethane product was trans-1,2-dibromo-1,2-diphenylethane
Which is the correct name for the followingcompound?A. 1-methyl-2-chlorocylohex-2-eneB. 1-chloro-2-methylcylohex-2-eneC. 2-methyl-3-chlorocyclohexeneD. 6-chloro-1-methylcylohexeneE. 3-chloro-2-methylcyclohexene
Does the data provide evidence for the claim that the reaction of Br2 with alkenes proceeds via anti‐addition? The mleting point of the product was found to be 234.5-235.5C chemical reaction: trans-stilbene+pyrimindine tribromide --->acetic acid 1,2-di bromo-1,2-diphenylethane
For #5 I need to know how to find all the r/s. The 1,3,5 trimethylhexane confuses me on how to find the R/S