IUPAC Name is :-
1-Ethyl-2,3-dimethylcyclopentane
The more substituents the alkenes have, the more stable they are that is the more substituted alkene is most stable.So stability order is :-
iii>ii>i
Most stable carbocation will be formed at Carbon B because at this carbon carbon is tertiary carbocation and it is also resonance stabilise
C31H64 is an example of parrafin wax so option e is correct
What is the IUPAC name of the following compound? 4 Rank the following alkenes from most...
1) What is the IUPAC name for the following compound? A) 6-Ethyl-6-heptene C) 2-Ethyl-1-heptene B) 2-Ethyl-1-octene D) 6-Ethyl-1-heptene 2) Label each C-C double bond in Kavain, a naturally occurring relaxant, as Eor Z. CH5 Kavain A) I = E and II = E CI= Z and II = E B) I = Z and II = Z D) I = E and II = Z 3) Which of the following statements about alkenes is not true? A) They are less...
8. What is the IUPAC name for the following compound? A) 2,3-Dimethyl-4-sec-butylheptane B) 4-sec-Butyl-2,3-dimethylheptane C) 3,5,6-Trimethyl-4-propylheptane D) 2,3,5-Trimethyl-4-propylheptane 9. Rank the conformers of butane in order of decreasing stability, putting the most stable first. CH3 Онс сн сн, H CH CH н, сH, н" CH3 Н. H FH H H н H H H н H H IV C) II> III> I> IV D) I>IV> II>II A) IV>I>II> III B) IV>1>1II> II 10. Which of the following chair conformations represents...
I.
name the following compounds
II. write structures for each of the followong
structires
III.Arrange alkenes from most to least stable
IV. if rearrangement is expected, draw rearranged structure
for wach carbocation
V.
PLEASE HELP, ive been struggling in organic and this is the
review for our 3rd exam. if i can get help (and explanations) for
1-4 it would be a big help
CHM 2210 Examination 3 11/02/18 Directions: Please supply all answers in the spaces provided on both...
1. Give the IUPAC name for the following compound (5 pts): 2. Rank the following alkenes in order of increasing stability (5 pts): 3. Draw the mechanism and predict the product for each of the following reactions. HBr
SE ATO 1800A . Rank the following resonance structures from MOST to LEAST stable a. III > I > II b. II > I > III c. II > III >I d. I > II > III I > III > II
For each pair of species, predict which is the stronger base? 5. Он or 1. 2. or В в NH NH (a) (b) 6. Rank the following from most stable to least stable. 2. 3. 4. Нас Н-с O H -н CH H CH,сH, сн,сн CH,CH 7. Which cation would be the most stable? А. В. C. D. What is the order of increasing contribution to the resonance hybrid? 8. CF3 ÇF3 CF3 I II III
QUESTION 24 Rank the following alcohols in decreasing order of acidity. ROH ON OH ОН NC II III A) I>III>II B) III>II>I C) II>III>I DI>II>III A B C D QUESTION 23 How would you use 'H NMR spectroscopy to distinguish between the following two compounds? W H II A) I=3 signals & II=2 signals B) 1-4 signals & I1=3 signals C) 1=5 signals & 11=3 signals A B OC QUESTION 22 Provide the reagents necessary to prepare the following compound...
NA afte. 9 Select the most stable conformation for trans-1-tert-butyl-3-methylcyclohexane. н D A 10. Which of the following compounds are optically active [will rotate plane polarized light (is chiral)]? CIL CI CI CI C/. CI A CI CI В D С 11. Rank absorption of the indicated bonds in decreasing (highest to lowest) wavenumber. II н x III a) III> II>I b) I> II III OH c) II>I> IlI d) III I> II но, но—н 12. How many stereocenters are...
Which of the following reaction is a syn addition(s)? A. Hydroboration-oxidation of alkenes B. Hydrohalogenation reaction of alkenes C. Dihalogenation reaction alkenes D. Halohydrin formation reaction 7. Consider the three compounds below: 1. CH CH OCH CH, II. CH CH CH CH CH, M.CH, CH2CH2CH2OH The two most similar in boiling point are: A. I and II B . I and III C. II and III D. There is no way to judge since no boiling point is provided for...
Need help understanding why? Thanks!
9. Rank the following from most to least acidic CI COOH COOH coOH COOH IV A. I II III >IV B. II I IV> III C. III IV II > I D. IV III I > II E. III IV I II 10. Which hydrogen is the most acidic in the molecule shown below? C A 11. Why are ketones less reactive than aldehydes? A. Ketones are less sterically hindered. B. Carbonyl carbon of ketones...