![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)
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.
![R)-2 -Iodobutane is treated with NaI in acetone and allowed to stand a long time.The product eventually formed is: R)-2 -Iodobutane is treated with NaI in acetone and allowed to stand a long time.The product eventually formed is:](https://search-static.byjusweb.com/question-images/toppr_ext/questions/770319_740334_ans_d3ab192fa851487a9971b973996f3918.png)
R)-2 -Iodobutane is treated with NaI in acetone and allowed to stand a long time.The product eventually formed is:
Scheme 1 Synthesis of N 6-benzoyl-AdoHyc. (a) NaI-acetone, 69%. (b)... | Download Scientific Diagram
![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
![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
![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
![organic chemistry - Why does d/l-2,3-dibromobutane on reaction with NaI/ acetone give cis-2-butene? - Chemistry Stack Exchange organic chemistry - Why does d/l-2,3-dibromobutane on reaction with NaI/ acetone give cis-2-butene? - Chemistry Stack Exchange](https://i.stack.imgur.com/0DVlr.png)
organic chemistry - Why does d/l-2,3-dibromobutane on reaction with NaI/ acetone give cis-2-butene? - Chemistry Stack Exchange
![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)