choose the most stable isomer from each list 13. [06 pts.] Circle the most stable isomer from each list.
circle the most stable isomer from each list 3. [06 pts.] Circle the most stable isomer from each list. A.
Circle the most stable and underline the least stable carbocations. 1.(1 pt each) Circle the most stable and underline the least stable carbocations below. 3- a.
1. Draw the MOST stable and the LEAST stable isomer of 3- chloro -4- methylhexane by drawing Newman Projections looking down the bond between Carbon -3 and Carbon-4 2. Circle the most acidic Hydrogen and then explain its acidity as needed with structures and sentençes NH2 OH
List the following carbocations in each set in order from most stable (numbering from 1) to least stable (numbering to 3): PLEASE EXPLAIN! primary, secondary, tertion least 2) (3 points) List the following carbocations in each set in order from most stable (numbering from 1) to least stable (numbering to 3): a. CH3CH2CCH CH3CH2CHCH2 CH3CH2CH2CH2 CHE b. CH3CHCHCH; CH3CHCHCH2 CH3CHCHCH? CH3
1. Rank the following cyclic alkanes from most stable (1) to least stable (4). (2 pts) 2. From the sawhorse projections below, circle the highest energy conformation for ethane. (2 pts) HH Hн HHH HH Hy Yo ΗΜΗ 3. Circle the chair conformation below that represents the lowest energy conformation for cis-1,3- dimethylcyclohexane? (2 pts) SSSSSS 4. In the figure below, identify the Newman projections by the letter (A, B, C, or D) which best describes each conformation for 1-chloropropane....
Draw the most stable isomer by Newman projection and chair structure of the ring.
draw the most stable and least stable isomer of 3-chloro-4-methylhexane by drawing Newman Projections looking down the bond between carbon-3 and carbon-4
DRAW THE MOST STABLE AND LEAST STABLE ISOMER OF 3-isopropyl-4-methoxy herane BY DRAWINO NEMAN PROJECTIONS LOOKING DOWN THE BOND BETWEEN CARBON-3 AND CARBON-Y
Rank the following allylic carbocations in order from least stable to most stable THEN justify your answer in words: 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.
please explain/walkthrough! Problem 1 (30 pts) a) Circle the radical that is most stable. b) Order the compounds in terms of increasing oxidation state (1 highest, 3- lowest) он c) The reaction below is an example of.... heat 2 b) substitution a) addition d) heterolytic cleavage c) homolytic cleavage d) Circle the compound with the most acidic protons. H H c=C CHз CH3CH2CH3 Нас-СЕС-н H