(a)
Interpretation:
Products formed when conjugate base of diethyl malonate reacts with the given set of electrophiles need to be identified.
Concept introduction:
Diethyl malonate in presence of a strong base undergoes deprotonation to form conjugate base. This can function as a nucleophile and it can reacts with electrophile to give the respective products after acidic work-up.
To identify : To identify the product formed when the conjugate base of diethyl malonate react with the given electrophile.
(b)
Interpretation:
Products formed when conjugate base of diethyl malonate reacts with the given set of electrophiles need to be identified.
Concept introduction:
Diethyl malonate in presence of a strong base undergoes deprotonation to form conjugate base. This can function as a nucleophile and it can reacts with electrophile to give the respective products after acidic work-up.
To identify : To identify the product formed when the conjugate base of diethyl malonate react with the given electrophile.
(c)
Interpretation:
Products formed when conjugate base of diethyl malonate reacts with the given set of electrophiles need to be identified.
Concept introduction:
Diethyl malonate in presence of a strong base undergoes deprotonation to form conjugate base. This can function as a nucleophile and it can reacts with electrophile to give the respective products after acidic work-up.
To identify : To identify the product formed when the conjugate base of diethyl malonate react with the given electrophile.
(d)
Interpretation:
Products formed when conjugate base of diethyl malonate reacts with the given set of electrophiles need to be identified.
Concept introduction:
Diethyl malonate in presence of a strong base undergoes deprotonation to form conjugate base. This can function as a nucleophile and it can reacts with electrophile to give the respective products after acidic work-up.
To identify : To identify the product formed when the conjugate base of diethyl malonate react with the given electrophile.
(e)
Interpretation:
Products formed when conjugate base of diethyl malonate reacts with the given set of electrophiles need to be identified.
Concept introduction:
Diethyl malonate in presence of a strong base undergoes deprotonation to form conjugate base. This can function as a nucleophile and it can reacts with electrophile to give the respective products after acidic work-up.
To identify : To identify the product formed when the conjugate base of diethyl malonate react with the given electrophile.
(f)
Interpretation:
Products formed when conjugate base of diethyl malonate reacts with the given set of electrophiles need to be identified.
Concept introduction:
Diethyl malonate in presence of a strong base undergoes deprotonation to form conjugate base. This can function as a nucleophile and it can reacts with electrophile to give the respective products after acidic work-up.
To identify : To identify the product formed when the conjugate base of diethyl malonate react with the given electrophile.
(g)
Interpretation:
Products formed when conjugate base of diethyl malonate reacts with the given set of electrophiles need to be identified.
Concept introduction:
Diethyl malonate in presence of a strong base undergoes deprotonation to form conjugate base. This can function as a nucleophile and it can reacts with electrophile to give the respective products after acidic work-up.
To identify : To identify the product formed when the conjugate base of diethyl malonate react with the given electrophile.
(h)
Interpretation:
Products formed when conjugate base of diethyl malonate reacts with the given set of electrophiles need to be identified.
Concept introduction:
Diethyl malonate in presence of a strong base undergoes deprotonation to form conjugate base. This can function as a nucleophile and it can reacts with electrophile to give the respective products after acidic work-up.
To identify : To identify the product formed when the conjugate base of diethyl malonate react with the given electrophile.
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Chapter 21 Solutions
ORGANIC CHEMISTRY (LL)-W/WILEYPLUS
- What kind of holes are not generated when solid-state particles adopt a close packing pattern? Group of answer choices tetrahedral cubic octahedral None of the other choices are correctarrow_forwardFor the reaction below: 1. Draw all reasonable elimination products to the right of the arrow. 2. In the box below the reaction, redraw any product you expect to be a major product. 田 Major Product: Check ☐ + I Na OH esc F1 F2 2 1 @ 2 Q W tab A caps lock S #3 80 F3 69 4 σ F4 % 95 S Click and drag to sta drawing a structure mm Save For Later 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use GO DII F5 F6 F7 F8 F9 F10 6 CO 89 & 7 LU E R T Y U 8* 9 0 D F G H J K L Z X C V B N M 36arrow_forwardProblem 7 of 10 Draw the major product of this reaction. Ignore inorganic byproducts. S' S 1. BuLi 2. ethylene oxide (C2H4O) Select to Draw a Submitarrow_forward
- Feedback (4/10) 30% Retry Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the arrows to draw the reactant and missing intermediates involved in this reaction. Include all lone pairs and charges as appropriate. Ignore inorganic byproducts. Incorrect, 6 attempts remaining :0: Draw the Reactant H H3CO H- HIO: Ö-CH3 CH3OH2* protonation H. a H (+) H Ο CH3OH2 O: H3C protonation CH3OH deprotonation > CH3OH nucleophilic addition H. HO 0:0 Draw Intermediate a Xarrow_forwardCan I please get the blank spaces answered/answers?arrow_forward1. Identify the following alkenes as E or Z NH₂ Br 2. Draw the structures based on the IUPAC names (3R,4R)-3-bromo-4-fluoro- 1-hexene (Z)-4-bromo-2-iodo-3-ethyl- 3-heptene تر 3. For the following, predict all possible elimination product(s) and circle the major product. HO H₂SO4 Heat 80 F4 OH H2SO4 Heat 어요 F5 F6 1 A DII 4 F7 F8 F9 % & 5 6 7 * ∞ 8 BAB 3 E R T Y U 9 F D G H J K O A F11 F10arrow_forward
- Draw the major product of this reaction. Ignore inorganic byproducts. ○ O 1. H₂O, pyridine 2. neutralizing work-up a N W X 人 Parrow_forward✓ Check the box under each molecule that has a total of five ẞ hydrogens. If none of the molecules fit this description, check the box underneath the table. tab OH CI 0 Br xx Br None of these molecules have a total of five ẞ hydrogens. esc Explanation Check caps lock shift 1 fn control 02 F2 W Q A N #3 S 80 F3 E $ t 01 205 % 5 F5 & 7 © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility FT * 8 R T Y U כ F6 9 FIG F11 F D G H J K L C X V B < N M H option command P H + F12 commandarrow_forwardDraw the major product of this reaction. Ignore inorganic byproducts and the carboxylic acid side product. O 1. CHзMgBr (excess) 2. H₂O ✓ W X 人arrow_forward
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