![From each of the following pairs select the compound that will react faster with sodium iodide in acetonea 2 Chloropropane or 2 bromopropane I IIb 1 Bromobutane or 2 bromobutane I II From each of the following pairs select the compound that will react faster with sodium iodide in acetonea 2 Chloropropane or 2 bromopropane I IIb 1 Bromobutane or 2 bromobutane I II](https://df0b18phdhzpx.cloudfront.net/ckeditor_assets/pictures/1213533/original_80.png)
From each of the following pairs select the compound that will react faster with sodium iodide in acetonea 2 Chloropropane or 2 bromopropane I IIb 1 Bromobutane or 2 bromobutane I II
![a) Give the product of debromination with NaI in acetone solution of the following. (i) Erythro or meso -2,3- dibromobutane (ii) Threo or `(+-)-2,3-` - Sarthaks eConnect | Largest Online Education Community a) Give the product of debromination with NaI in acetone solution of the following. (i) Erythro or meso -2,3- dibromobutane (ii) Threo or `(+-)-2,3-` - Sarthaks eConnect | Largest Online Education Community](https://learnqa.s3.ap-south-1.amazonaws.com/images/1612526693462866989mg1S5wSaB6Os7fll.png)
a) Give the product of debromination with NaI in acetone solution of the following. (i) Erythro or meso -2,3- dibromobutane (ii) Threo or `(+-)-2,3-` - Sarthaks eConnect | Largest Online Education Community
![NAI-150A-1 - 1,4-Naphthoquinone (cas 130-15-4) Solution, 100 µg/mL, in acetone - Ultra Scientific Italia NAI-150A-1 - 1,4-Naphthoquinone (cas 130-15-4) Solution, 100 µg/mL, in acetone - Ultra Scientific Italia](https://www.ultrasci.it/wp-content/uploads/2021/09/ORG-1-Sito.png)
NAI-150A-1 - 1,4-Naphthoquinone (cas 130-15-4) Solution, 100 µg/mL, in acetone - Ultra Scientific Italia
![Here, $\\text{1-4 dichlorohexane (1 mole) + NaI (1 mole)}\\xrightarrow{ Acetone}$ Product of the reaction is:(a) \n \n \n \n \n (b)\n \n \n \n \n (c) \n \n \n \n \n (d)\n \n \ Here, $\\text{1-4 dichlorohexane (1 mole) + NaI (1 mole)}\\xrightarrow{ Acetone}$ Product of the reaction is:(a) \n \n \n \n \n (b)\n \n \n \n \n (c) \n \n \n \n \n (d)\n \n \](https://www.vedantu.com/question-sets/8a9119e4-80e4-45b7-83c0-010cae2a4ed6709535833189690645.png)
Here, $\\text{1-4 dichlorohexane (1 mole) + NaI (1 mole)}\\xrightarrow{ Acetone}$ Product of the reaction is:(a) \n \n \n \n \n (b)\n \n \n \n \n (c) \n \n \n \n \n (d)\n \n \
![SOLVED: What is the predicted product for the reaction shown? 1. NaI/acetone 2. NaCN/DMF CN OCN Oâ‚‚ SOLVED: What is the predicted product for the reaction shown? 1. NaI/acetone 2. NaCN/DMF CN OCN Oâ‚‚](https://cdn.numerade.com/ask_images/415f77bceec64de1983def3bb5cfccbe.jpg)
SOLVED: What is the predicted product for the reaction shown? 1. NaI/acetone 2. NaCN/DMF CN OCN Oâ‚‚
![SOLVED: What is the major product for the following reaction? 1. NaI, acetone 2. NaOH, EtOH, heat CI B) E) SOLVED: What is the major product for the following reaction? 1. NaI, acetone 2. NaOH, EtOH, heat CI B) E)](https://cdn.numerade.com/ask_images/959c1d17803a48f289d489963344517e.jpg)
SOLVED: What is the major product for the following reaction? 1. NaI, acetone 2. NaOH, EtOH, heat CI B) E)
![te Nai Acetone 1 → Product Acetone > Product. * Product and reactant related as (1) Identical molecules 21 Diastereomers (3) Enantiomers (4) Two different molecules te Nai Acetone 1 → Product Acetone > Product. * Product and reactant related as (1) Identical molecules 21 Diastereomers (3) Enantiomers (4) Two different molecules](https://toppr-doubts-media.s3.amazonaws.com/images/5603231/9823529a-8a7a-4303-9e9a-99f1baf89e5d.jpg)
te Nai Acetone 1 → Product Acetone > Product. * Product and reactant related as (1) Identical molecules 21 Diastereomers (3) Enantiomers (4) Two different molecules
Scheme 1 Synthesis of N 6-benzoyl-AdoHyc. (a) NaI-acetone, 69%. (b)... | Download Scientific Diagram
![Assertion :Optically active 2-iodobutane on treatment with NaI in acetone undergoes racemization. Because Reason: Repeated Walden inversions on the reactant and its product eventually give a racemic mixture. Assertion :Optically active 2-iodobutane on treatment with NaI in acetone undergoes racemization. Because Reason: Repeated Walden inversions on the reactant and its product eventually give a racemic mixture.](https://search-static.byjusweb.com/question-images/toppr_ext/questions/421322_263023_ans.png)