Identify the configurations around the double bonds in the compound Н Нас, CHз CHз CH3 Н...
Question 10 of 28 > Identify the configurations around the double bonds in the compound. H3C CH2 CH₃ H₃C Answer Bank neither trans CLS
Identify the configurations around the double bonds in the compound below. Selected bonds will be highlighted green. Be sure that you select only double bonds. Donot select atoms. Select the double bonds in the cis configuration. If Select the double bonds in the trans configuration. If there are no trans double bonds, do not select any there are no cis double bonds, do not select any bonds bonds. CH3 CH3 H3C CH3 H3C CH CH3 CH3 CH3 CH3 CH2 CH2...
Indicate whether the pair of structures shown represent stereoisomers, constitutional isomers, different conformations of the same compound, or the same conformation of a compound viewed from a different perspective. Note that cis, trans isomers are an example of stereoisomers CHз Нас Нас. Н.с ОН Он same conformation Cl- C CI Cl CI CI CН3- CH3 CHз Н H CH3 H OH H НО. H CНз- OH H OH CНз constitutional isomers I I T -I Indicate whether the pair of...
Select the double bonds in the cis configuration. If there are no cis double bonds, do not select any bonds. Select the double bonds in the trans configuratic Map there are no trans double bonds, do not select any bonds. H сн. H HC CH3 CH3 Н.С. CH3 CH3 CH3 CH3 сна CH2 CH2 HO HO Name the following alkenes using systematic names. H3C CH3 H3C H CH2 CH2 CH3 CH2 H3c1 -CH₂ Br CH2 CHE CH₂ H сн.
write the iupac name of the following compound Hс Н ал н У-Br ыiт он Нас 6. CH3 н У Br H Н 7. CHs н н - Br Hас 8 CHз Н HаC -Br HС
Give the IUPAC name or common name for each compound о 2. CH3 Н,с Cl "CHз CH3 Н,с b. а. CH3 - CH3 d. С. Draw the structures correspond ing to each name: a. 4-methylheptanen itrile b. Cyclohexyl-2-methylbutanoate 3.
2) Order the following alkenes from most stable to least stable Нас Нас с-сн, н,с Hас +C- Нас н CHs -CH3 H Hе most stable least stable (a) I (b) I (c) I ll (d) 7) Order the following C-H bonds from strongest to weakest. strongest weakest (a) (b) (c) II (d) 8) Which of the following is represents the lowest energy transition state for the addition of BH, to 2-methyl-1-propene? quCH «сHs нСи Нас (b) (a) Нив--н H H...
For each pair of isomers in the table below, indicate the type of isomerism that is present from the following list: chain, position, functional group, geometric (cis-trans), enantiomer 2. OH CH3CH2CH2OH CHяCHCHз CH3CH2OH CH30CH3 COOH HOOC Нас н он Hu C CHз но CI H H H CH3 CH3CH2CH2CH3 CH3CHCH3 3. Write the systematic IUPAC name of the compound:
CH3 CH2 CH CH Нас—С—С CH3 Spell out the full name of the compound Request Answer Submit Part D Interactive 3D display mode сн, —с—с—с—сн, н Н,с— Hа CH3
сн, Нас 12-addition products (direct addition) CH2 CH3 Н,с Н-с CH CI HCI CH2 Cн Н.с 1,4-addition products (conjugate addition) Cн CH3 Нас Н.С CI Electrophilic addition to an alkene proceeds via Markovnikov regiochemistry due to the formation of the more stable carbocation intermediate. In the case of conjugated dienes, that is dienes that are separated by one sigma bond, the carbocation that is formed is stabilized additionally by resonance. Addition of the nucleophile to the carbocation intermediate can therefore...