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The decresing fugacity order of the foll...

The decresing fugacity order of the following is:
i. `Me_(2)N - Nme_(2)`, ii. `MeNH-NHMe`
iii. `H_(2)N - NH_(2)`, iv. `NH_(3)`

A

`(i) gt (ii) gt (iii) gt (iv)`

B

`(iv) gt (iii) gt (ii) gt (i)`

C

`(iv) gt (iii) gt (i) gt (ii)`

D

`(iii) gt (iv) gt (ii) gt (i)`

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The correct Answer is:
To determine the decreasing fugacity order of the given species, we need to analyze their basic strengths since the fugacity order is inversely related to the basic strength. Here are the steps to find the solution: ### Step 1: Identify the Compounds The compounds given are: 1. \( Me_2N - NMe_2 \) (Dimethylhydrazine) 2. \( MeNH - NHMe \) (Methylhydrazine) 3. \( H_2N - NH_2 \) (Hydrazine) 4. \( NH_3 \) (Ammonia) ### Step 2: Determine Basic Strengths Basic strength is influenced by the number of electron-donating groups and the availability of lone pairs on the nitrogen atoms. - **Dimethylhydrazine (i)**: Has two nitrogen atoms each bonded to two methyl groups. The methyl groups are electron-donating, which increases the basicity. - **Methylhydrazine (ii)**: Has two nitrogen atoms, but only one is bonded to a methyl group. This makes it less basic than dimethylhydrazine. - **Hydrazine (iii)**: Has two nitrogen atoms with no methyl groups. It is less basic than both dimethylhydrazine and methylhydrazine. - **Ammonia (iv)**: Has only one nitrogen atom and no electron-donating groups. It is the least basic of all. ### Step 3: Rank the Basic Strengths Based on the above analysis, we can rank the basic strengths from strongest to weakest: 1. \( Me_2N - NMe_2 \) (most basic) 2. \( MeNH - NHMe \) 3. \( H_2N - NH_2 \) 4. \( NH_3 \) (least basic) ### Step 4: Determine the Fugacity Order Since the fugacity order is inversely related to the basic strength, we reverse the order: 1. \( NH_3 \) (best leaving group) 2. \( H_2N - NH_2 \) 3. \( MeNH - NHMe \) 4. \( Me_2N - NMe_2 \) (poorest leaving group) ### Final Fugacity Order Thus, the decreasing fugacity order is: \[ NH_3 > H_2N - NH_2 > MeNH - NHMe > Me_2N - NMe_2 \] ### Answer The decreasing fugacity order of the given compounds is: \[ NH_3 > H_2N - NH_2 > MeNH - NHMe > Me_2N - NMe_2 \] ---

To determine the decreasing fugacity order of the given species, we need to analyze their basic strengths since the fugacity order is inversely related to the basic strength. Here are the steps to find the solution: ### Step 1: Identify the Compounds The compounds given are: 1. \( Me_2N - NMe_2 \) (Dimethylhydrazine) 2. \( MeNH - NHMe \) (Methylhydrazine) 3. \( H_2N - NH_2 \) (Hydrazine) 4. \( NH_3 \) (Ammonia) ...
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CENGAGE CHEMISTRY ENGLISH-AROMATIC COMPOUNDS AND ALKYL AND ARYL HALIDES -Exercises Single Correct
  1. The decrasing basic order of the following is: i. Me(2)N - NMe(2), i...

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  2. Decreasing nucelophilic order of the following is: i. Me(2)N - Nme(2...

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  3. The decresing fugacity order of the following is: i. Me(2)N - Nme(2)...

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  4. underset("Specific rotation" = +50^(@))(Ph-CH(OH)CH(3)) overset(SOCl(2...

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  5. underset("Specific rotation" = +50^(@))(Ph-CH(OH)CH(3)) overset(SOCl(2...

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  6. underset("Specific rotation" = +50^(@))(Ph-CH(OH)CH(3)) overset(SOCl(2...

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  7. underset("Specific rotation" = +50^(@))(Ph-CH(OH)CH(3)) overset(SOCl(2...

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  8. CH(3) - CH(Cl) - C(2)H(5) overset(Alc.KOH)(rarr) CH(3) - CH = CH - CH(...

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  9. Alkyl halides can be obtained by all methods except

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  10. Neopentyl chloride on reaction with ethanolic KOH is likely to give

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  11. In the reaction CH(3)C equiv C^(-)Na^(+) + (CH(3))(2) CHCl rarr Prod...

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  12. In order to get ethanethiol from bromoethane, the reagent used is :

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  13. For the preparation of chloroethane,

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  14. X on treatment with sodium hydroxide followed by the addition of silve...

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  15. Which of the following cannot be used for the preaparation of iodofro...

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  16. Which of the following hladies is capable of exhibitin enantiomerism?

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  17. A suspension of CaOCl(2) in water is heated with ethanol, the product ...

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  18. Pick up the correct statements about alkyl halides.

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  19. Which of the following is a geminal dihalide ?

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  20. C(2)H(5)I overset(AgNO(2))rarr underset(("major product"))("X. Here X"...

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