2. Name the following compounds:CH3CH3CH2H3CCHCHCHCH3CH3Ia.CH 3CH₂CH 3CH 3CH₂CHCHCHCH3CH2CHb. CH 3CH3c. H&CCH-CHCH33H3C-C-BrCH3-CId.e.CH3CH2ICH-FCH₂CH2CH2 CH 3f.CH 3CHCH 3CH2CH₂CHCH₂CH3'CHCH3g.

Answered: Image /qna-images/answer/2eb10efd-f580-4deb-ad63-263f53ea895a.jpg

Answered: 2. Name the following compounds: CH3…

Chemistry

10th Edition

ISBN:9781305957404

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

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

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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32. С-С-С Which of the following is another correct representation of the compound above? Oa. CH2-CH2-CH2 Ob. CH3-CH3-CH3 Oc. CH3-CH2-CH3 Od. CH4-CH3-CH4
Name the following compounds. CH3 H3C a. b. H FC C -C - H- н н С. HO
ch1
1. You have the tools to accomplish one of the early synthesis of a major alkaloid. Porantherine (molecule M) is the main alkaloid of the low woody shrub Poranthera corymbosa distributed in the southwest. The following questions pertain to the attached synthetic scheme (J. Am. Chem. Soc. 1974, 96, 6516). The are key steps that utilize an aldol-like mechanism to close three rings (A) What kind of transformation is the D → E step; show NO mechanism, but what was added to D? Hint: molecule E clearly has a terminal alkene and ketone, but what is the third functional group (it's not another alkene)? You've done the mechanism for making this functional group in chapter 20. (B) The E F transformation is rather elegant and it is promoted by an acid (toluenesulfonic acid). It involves formation of an enol (tautomerization) followed by protonation on the C=C bond in the ring to form a resonance- stabilized carbocation. Show the mechanism of this cyclization starting from the enol (i.e. double…
Н3С H3C- H3C H3C- CH3 H3C H3C H3C CH3 CH3 a. Name: CH3 CH3 b. Name: CH3 CH3 CH3 CH3 -CH3 c. Name: CH3 d. Name: e. Name:
a. (CH3)3C-N=N: b. .CH3 + CH3 Question 6: Use curved arrows to show the movement of electrons in each equation. C. CH₂-C+ 1 CH3 d. HÖ-ÖH -CH-3 SAYER Br: HO CH3 2 HÖ- (CH³)3C+ + =N=N: CH3-CH3 CH₂ CH₂-C-Br: CH3 O
a. b. C. CH,CH-CH-CH-CH₂OH CH,CHCH,CHCH,CH3 CH₂CHCH CHCH CH₂ CH3 OH OH Br d. OH CH,CHCH2CH3 OH f. CH₂ CH₂-CH-CH, CH- h. i. OH OH CH,CHOCH-CH-CHCH, CH3 j. OH Br CH3 Question: Name the following compounds using systematic/IUPAC nomeclature:
Name these compound
Draw three molecules of each compound below.a. propane, CH 3 CH 2 CH 3b. heptane, CH 3 CH 2 CH 2 CH 2 CH 2 CH 2 CH 3c. 1-propanol, CH 3 CH 2 CH 2 OHd. 1-heptanol, CH 3 CH 2 CH 2 CH 2 CH 2 CH 2 CH 2 OH
the composition exhibiting the cis-trans isomer is B. CH=C-CH,Br D. CHBR=CBr-CH, A. HCOOBr C. CBr,=CBr-CH3
3. CH3-CHUCH-c-CI Class number: Date: CH3 CH3 4. CH3- CH2-C-O- CÖH 5. CH3- CH2-C-O- CH3 6. H- C-O-CH3 7. CH3-CH2-CH2-O-C-CH3 blon simolna CH3 bo ainclam ons bo oi u 8. CH,-CH,- C-o-CH.CH, n inlooue bna bos ohu 9. OH OH CH3 10. HO-CCH- CH-CH-cM how foum 1I- Draw a condensed structural formula for each cf the following compounds: 1. Valeric acid 2. Acetic acid 3. a-chlorobutyric acid 4. B-Bromocaproic acid 5. Methyl formate
Which molecule is a complete organic molecule (i.e. all atoms are shown correctly)? A H. c=C–C= C–H H C H. C=C-C-C-H | H. H. C H. C- D H. нн . C С —С—Н C=C–C- C-H H H. ОН Н А I-0-I エーO I-Ú-I I-U-I I-U-I エー○

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2. Name the following compounds: CH3 CH3 CH2 H3C CH CH CH CH3 CH3 I a. CH 3 CH₂ CH 3 CH 3 CH₂ CH CH CH CH3 CH2 CH b. CH 3 CH3 c. H&C CH-CH CH33 H3C-C- Br CH3 -CI d. e. CH3 CH2 I CH-F CH₂ CH2 CH2 CH 3 f. CH 3 CH CH 3 CH2 CH₂ CH CH₂ CH3 'CH CH3 g.