Of each of the following pairs of compounds, identify the one which would be the more stable, and give a justification???
Of each of the following pairs of compounds, identify the one which would be the more...
3.6: Which of the following compounds can exist as cis–trans isomers? Draw each cis–trans pair. (a) CH3CH=CH2 (b) (CH3)2C=CHCH3 (c) ClCH=CHCl (d) CH3CH2CH=CHCH3 (e) CH3CH2CH=C(Br)CH3 (f) 3-Methylhept-3-ene The answer is c, d, e ,f but I'm not sure how it works
4.51 Draw both chair conformations for each of the following compounds. In each case, identify the more stable chair conformation: (a) Methylcyclohexane (b) trans-1,2-Diisopropylcyclohexane (c) cis-1,3-Diisopropylcyclohexane (d) trans-1,4-Diisopropylcyclohexane
Which of the following pairs of compounds are
cis-trans isomers?
Which of the following pairs of compounds are cis-trans isomers? CH сн, н A. and сн, Н сн, H В. н CH and н Cн, Н C. сн, сн, CH and СH, сн.CH, CH н D. and -CH CH-CCH н Н,с. CH Cн, H and E. Cн, н н H T LL
Draw both chair conformations for each of the following compounds. In each case, identify the more stable chair conformation: (a) Methylcyclohexane (b) trans-1,2-Diisopropylcyclohexane (c) cis-1,3-Diisopropylcyclohexane (d) trans-1,4-Diisopropylcyclohexane
7.66 Predict which member of each of the following pairs of compounds will be more soluble in vegetable oil: a. NH3 or CH,CH2 CH2 CH,CH3 b.NaCl or CH,CH2OCH2CH3 c. cyclopentane or CH,CH2NH d. CH OH or CH,OCH when you wipe it
i need help on both questions...
12. Which one of the following compounds is more likely to have its OH bond broken? Why? OH Н.С. a. CHE H O HC-C H OH b. 13. Which one of the following compounds reacts with C2H5OH to produce the ester CH.COOC2Hs? Write the balanced equations, showing the reactants and the products. CH3CHO CH3COCH CH3COOH CHOCH.
identify which compound is more acidic and explain your choice. or each of the following compounds, Make sure you include structures of these which compounds in your answers ounds, 1. F (e) 24-Dimethy-3,5-hepanedione or 4, 4-Dimethy)-3,5-heptanedione (b) 1.2-Cyclopentanedione or 1,3-cyclopentanedione 2. When 2-hepten-4-one is treated with LDA, a proton is removed from one of the gamma (z) positions. identily which gamma position is deprotonated, and explain why the y proton is the most acidie proton in the compound. 3. Rank...
For each of the following pairs of compounds, circle the one that is the stronger acid: Which one of the following is the MOST stable carbocation? Circle the correct answer.
BOTH 4 and 5
4. For each pair of compounds, predict the one with a higher boiling point. Which compounds have zero dipole moments? a. cis-1,2-dichloroethene or cis-1,2-dibromoethene b. cis- or trans-2,3-dichlorobut-2-ene C. cyclohexene or 1,2-dichlorocyclohexene 5. Explain why each of the following alkenes is stable or unstable. a. 1,2-dimethylcyclopentene b. trans-1,2-dimethylcyclopentene
1. For each pair, circle the molecule with the lower pK and provide a brief explanation for your choice. wale wabon ---- 2. For each molecule, draw the two possible chair conformers and circle the preferred conformer. a) cis-1,3-dimethylcyclohexane trans-1,4-dimethylcyclohexane 3. Draw all distinct isomers of dimethylcyclopropane and show the relationship as enantiomer, diastereomer or meso. 4. In each of the following pairs of compounds one is chiral and the other achiral, Circle the chiral compound in each. a) CH,CHCH=CH...