None 2. Complete the following table:NameLewisstructurecondensed formulaCitastick structure2-chloropropaneH-C-C-C-HIIICH3CH CH3犬H C❘ HCl4-ethyl-3,5rdimethyloctaneisopropylcyclohexaneCH3CH₂ CH₂ CH3CH3CH2CH-CH-CH-CH323CH2CH3show clear workshow work. don'tgive Ai generatedsolution

In making the Lewis structures and condensed formula for hydrocarbons, make sure that carbon is…

Answered: 2. Complete the following table: Name…

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 50AP

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What Is the molecular formula of compound E?
• How do you differentiate the following pair of compounds by IR? H, H2 H H,c-Cc-CH, H2 1 H;C CH3 H2 H2 -CH3 H2 2 H,C H2 H2 H,c-Cc-CH, H2 H,c-CCECH H;C 4
2. Name the following alkenes: (a) (d) H H₂C C=C CH3 CHCH₂ CH3 H H c=c H3C H₂C=CHCHCH H 17 CH3 CH3 (b) (e) CH3 CH3CHCH₂CH₂CH H3C CH₂CH3 CH3CH₂CH₂ H₂C H C=C C=C C=C CH3 CH3 H H CH3 (c) CH₂ CH3 H₂C=CCH₂ CH3 (f) H₂C=C=CH CH3
(CH3)3C- (CHa)3C Br Br cis-1-bromo-4-tert-butylcyclohexane trans-1-bromo-4-tert-butylcyclohexane a. The cis and trans isomers of 1-bromo-4-tert-butylcyclohexane react at different rates with KOC(CH)3 to afford the same mixture of enantiomers A and B. Draw the structures of A and B. b. Which isomer reacts faster with KOC(CHa)g? Offer an explanation for this difference in reactivity. c. Reaction of cis-1-bromo-4-tert-butylcyclohexane with NAOCH3 affords C as the major product, whereas reaction of trans-1-bromo-4-tert-butylcyclohexane affords D as the major product. Draw the structures for C and D. d. The cis and trans isomers react at different rates with NaOCH3. Which isomer reacts faster? Offer an explanation for the difference in reactivity. e. Why are different products formed from these alkyl halides when two different alkoxides are used as reagents?
Explain why
Which of the following is a correct IUPAC name for the molecule shown. CH, H3C CH,CH,CH2 CH3 O (2E, 4Z)-4,5-dimethyloctadiene O (2E, 4E)-4,5-dimethyloctene • (2E, 4E)-4,5-dimethyloctadiene o (4E, 6E)-4,5-dimethyloctadiene (22, 4Z)-4,5-dimethyloctadiene
Pleaseeeeeeeeeeee explainnnnnnnn
Write down the IUPAC name and structure of the followings (i) HOH,C-CH = CH - CH,OH (ii) H.C =C-CH,-CH,-OH CH, (iii) HC = C-CH,-CH,-CH-CHO (iv) CH,COCOOH (v) CH,-CH-CHO OH ČCI (vi) CH,-CH- -ċ-CH-OCH, CH, CH, CH-CCI, (viii) CH CH = CH - COOH (vii) CH-CCI, (ix) CH,-CH-C-CH-OCH,CH, ÓCH, CH, (x) CH,-CH-CH, ОН Он ОН (xi) 2,4-dichlorohexane (xii) 6-methylhept-3-enal (xiii) 3-methylpentane-2,4-dione (xiv) 2-bromo-5-methylhexanoic acid (xv) 3-methylpentan-3-ol
Which of the following is the lower energy cyclohexane conformer? A-values: Br = 0.6 kcal/mol; isopropyl = 2.1 kcal/mol. Œ A B Br B Br
please do 13-18
N|ON|OU|G fic|Gb| app.101edu.co Maps YouTube 0³ A ℗ 2 F2 W S CO X G d B 2|GD|QC|GA Question 13 of 31 Provide the correct IUPAC name for the skeletal (line-bond) structure shown here. Stereochemistry is ignored. 1- 3- 2- 6- 4- 5- iso tert- di tri sec- cyclo pent hept non 99 MacBook Air # 3 > 0 80 F3 E D $ S4 Aav F4 R F 0, % 5 F F5 T G 6 Y & 7 H F7 U * 00 8 J DII F8 W G 1 CS UONEE 9 K F9 ) O O F10 L Done P Gri J F11 + (
(b) H CH2CH3 ·C. -CH2CH3 CH3 CH3OH (H)

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