Can someone please help me and explain I gave 1,3,2,4 **Instructions:**Rank each of the blue functional groups from least to most deactivating in an aromatic ring, with 1 being the least deactivating and 4 being the most deactivating.**Functional Groups:**1. **Acyl Group (C=O) attached to Benzene:** - Structure shows a carbonyl group (C=O) connected to a benzene ring. This group is moderately deactivating due to the electron-withdrawing nature of the carbonyl oxygen.2. **Hydroxyl Group (OH) attached to Benzene:** - Structure displays a hydroxyl group (OH) connected to a benzene ring. This group is activating, but it is listed here to identify its relative position among electron-withdrawing groups.3. **Carbamoyl Group (O=NH) attached to Benzene:** - Structure displays a carbamoyl group (O=NH) connected to a benzene ring. This group is moderately to strongly deactivating, reducing the electron density of the benzene ring.4. **Nitro Group (NO₂) attached to Benzene:** - Structure shows a nitro group (NO₂) connected to a benzene ring. This group is very strongly deactivating due to the strong electron-withdrawing effect of the nitro group.**Answer Options:**Fill in the blanks below each structure to rank them from least to most deactivating.1. ____2. ____3. ____4. ____ The task is to analyze the structures and decide their order of deactivation in electrophilic aromatic substitution reactions.

Answered: Rank each of the blue functional groups…

Rank each of the blue functional groups from least to most deactivating with 1 being the least and four being the most. ОН 'NH NO2

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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