Electron pairs C N O Erase H C N: CНз — с — Н Н —о — н Write the first step using curved arrows to show electron reorganization OH Na CN HC-C-CEN +H-CEN H Electron pairs Erase Н—о — СНз H CHз — с — н Н—о —СН3 Write the first step of hemiacetal formation using curved arrows to show clectron reorganization O-H НC -CH-C-H CHOH H O-CH 1. HBr 2. Mg, ether 3. 4. HCI, H2O Draw the...
name of following compounds.
CH3CCCH2CH2CHCCH2 H-C-H нннн н H-C-C-C-C-C-C-H нн| н H н-с-н н-С-н 1 н н-с-н 1 н HIC
n-butane Isobutane HH H-C-C-C C-HH Hl Primary n-butanol Primary isobutanol Secondary n-butanol Secondary isobutanol н-с-с-с-с-н Tertiary n-butanol Tertiary isobutanol Ethers Ethers have the same number and kinds of atoms as alcohols. However, they have very different physical properties and physiological effects. In the left box below, draw the structural formula for ethyl alcohol. Then construct a model. Next, take the model apart and rearrange it in the only other possible configuration to create dimethyl ether. Lastly draw the structural formula...
Compound Structure н ннн ТТІ H-C-C-C-C-H ТІТІ н ннн 2 H-CEC — — Н H 3 Н H 1 4 Hн Н H H ТІТІ нс-с-с-с-с-сесс-Н н ннн H н нннннннн ТТІ ТІГІ н-с-с-с -С-С -C-CH ТТТТТТТТІ й нннннннн S Table 4. Hydrocarbon Structures 2 Record the name of the compound structure in Data Table 1
D. Question 7 Which of the molecules below are structural isomers? Н Н H-C-H н-с-н Hннн Hнн Hн н-с-с-с-с-н н-с-с-с-с-н н-с-с-с-н нннн нннн ннн || Н Н-С-н н H н-с-с-с-н ннн 1 1 1 1 III III IV I and II I and IV I, III, and IV I and III
Q3. Draw the Condensed Structural formula for the following: H-C-H H-C-H - c-c-o - C - C- C- H - 0- Н "H-C-HH-C- HH-C-H Н
11. Indicate the order of stability CH н сн. Br CH сH, На н н. Br H H н н" Br н H н н н' Br н A В C D 12. Which of the following structures does NOT have tetrahedral geometry around any of its central central atoms. Use resonance to help explain A. В. с. D. = NH2 13. Is it theoretically possible to separate the pair of compounds below by distillation? Explain briefly CH CHs Br...
Lindlar's catalyst H- HC H-C-cEc-CHs h) HgSo, HC-HC-c c-H it + Н,о H,SO amu O HyCHC-cc-CH +H.O Н С k) 1. КОН HyC HC-CC CH hot KMnO 2. HC H,C HC CEC CHy cold KMnO
Lindlar's catalyst H- HC H-C-cEc-CHs h) HgSo, HC-HC-c c-H it + Н,о H,SO amu O HyCHC-cc-CH +H.O Н С k) 1. КОН HyC HC-CC CH hot KMnO 2. HC H,C HC CEC CHy cold KMnO
Name these organic compounds: compound name н С | | C1 —C—C— H . н CI CH Br — CH, —C— CH— Br . C1 —C— H
Which molecule has the shortest C-C bond? Select one: н Н а. C-C Н н Н н ob. н-с-с-Н н Н с. НЕСЕСЕН Not yet answered Marked out of 3.00 P Flag question Which one of the following compounds would have a specific rotation [a]p = 0 ? Br CH3 H -Br Н. -Br CH3 Br H CH3 -H Br CH3 H Br CH3 -Br -H CHE Br CH3 -Н -H CH,CHE a c d Select one: a. a b....