not use ai please Information: Markovnikov's rule states that "When adding a proton to an alkene, the proton adds to thealkene carbon with the most hydrogens". For example, CH2=CHCH2CH3 + HBr → CH3CHBrCH2CH3.2) For the structures below, label the alkene carbon with the most hydrogens with an 'M' and the alkene carbonwith the fewest hydrogens with an 'AM'. Then draw the products after addition of HBr.HBrHBr

Step 1: Step 2: Step 3: Step 4:

Answered: Information: Markovnikov's rule states…

World of Chemistry, 3rd edition

3rd Edition

ISBN:9781133109655

Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste

Chapter20: Organic Chemistry

Section: Chapter Questions

Problem 4STP

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a) Give the molecular formula and draw the skeletal structure for 3-bromo-3- methylhexane. b) Name (including E/Z stereochemistry) the FIVE alkenes that can produce 3-bromo-3- methylhexane on reaction with HBr. Draw the skeletal structure of each molecule.??? c) Define the type of stereoisomerism present in 3-bromo-3-methylhexane. Name and draw the tetrahedral representation of the two stereoisomers?. d) For the base-catalysed hydrolysis of 3-bromo-3-methylhexane (i.e. reaction with the nucleophile OH-): i) ii) iii) iv) State whether the reaction is likely to proceed by an SN1 or SN2 mechanism, and explain your choice Give the likely rate law for the reaction. Explain your choice. For the reaction intermediate, draw its structure and give the VSEPR description of the geometry at the reaction centre Give the names and draw the structures of the two reaction products. Explain your conclusions
Below is the structure for beta-carotene, a pigment found in plants and vegetables that give them their color. Determine how many alkenes are properly trans in the structure.
Pyrethrins, such as jasmolin II (shown below), are a group of natural compounds that are synthesized by flowers of the genus Chrysanthemum (known as pyrethrum flowers) to act as insecticides. CH3 CH2=CH-CH. CH-C- -HCS 0-CH, CH,-C H2C- ČH, Which is not a functional group or structural feature in jasmolin II? cycloalkane carboxylic acid ester alkene
"A cis alkene is more polar than a trans alkene, giving it a slightlyhigher boiling point and making it more soluble in polar solvents" Explain this statement ?
Organic Chemistry 1 (CHEM313)-Worksheet 02 1. Draw the structure of the molecule based on the IUPAC (systematic) name. cyclobutylcyclohexane 2,2,3,3-tetramethylheptane 3-ethyl-2,3-dimethylpentane 4,4,5-tripropyloctene 1,1,2,2,3,3-hexamethylcyclopropane 3-pentylcyclohept-1-ene 2-methyl-1-nitrobutane 4-methylhex-2-yne
Please draw the line structures for the C8H17+ carbocations that have the carbon skeleton below And please circle the most stable carbocation
These are different isomers for C4H8O. Which structure would not be an isomer of butanal?
c) For the IUPAC names below, provide an unambiguous structure! 1) (1R, 2R, 4S)-1,2-dibromo-4-methyl-cyclohexane 2) (2R, 3Z)-5-Fluoro-3-penten-1,2-diol
Draw skeletal structure:
2. Please draw out structure of the following compounds. 1) (Z)-1-chloro-3-ethyl-4-methyl-3-heptene 2) (E)-3-Ethyl-5-methyl-2-hexene
Draw the structure of 1,2,3-trimethylcyclohexene. ● Ⓡ Show stereochemistry only if given in the name. You do not have to explicitly draw H atoms. 8) $ #[ ] در ? ChemDoodleⓇ
What alkane, with molecular formula C7H16, forms seven monochlorinated products (disregarding stereoisomers) when heated with Cl2?

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