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CH(3)CH(2)-CH(2)-COOH overset("Red P" +...

`CH_(3)CH_(2)-CH_(2)-COOH overset("Red P" +Br_(2))toCH_(3)-CH_(2)-underset(Br)underset(|)(CH)-COOH`
This reaction is called

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To solve the question, we need to analyze the given reaction step by step. ### Step 1: Identify the Reactants The reactant provided is CH₃CH₂CH₂COOH, which is butanoic acid (a carboxylic acid). **Hint**: Look for the functional group in the compound to identify its class (in this case, a carboxylic acid). ### Step 2: Understand the Reaction Conditions The reaction is carried out in the presence of red phosphorus and bromine (Br₂). Red phosphorus is often used to facilitate halogenation reactions. **Hint**: Remember that red phosphorus can help in the halogenation of compounds, especially in the presence of halogens. ### Step 3: Identify the Alpha Carbon In the structure of butanoic acid, the carbon adjacent to the carboxylic acid group (COOH) is known as the alpha carbon. In this case, the alpha carbon is the third carbon in the chain. **Hint**: The alpha carbon is always the one directly next to the functional group in carboxylic acids. ### Step 4: Determine the Reaction Mechanism In this reaction, the hydrogen atom attached to the alpha carbon is replaced by a bromine atom (Br). This process is known as halogenation, specifically alpha halogenation because it occurs at the alpha carbon. **Hint**: Look for the substitution of hydrogen with a halogen at the alpha position to identify the type of reaction. ### Step 5: Identify the Product The product formed is CH₃CH₂CHBrCOOH, which is an alpha-bromobutanoic acid. **Hint**: The presence of the bromine atom at the alpha position indicates that the reaction has successfully occurred. ### Step 6: Name the Reaction The reaction described is known as the Hell-Volhard-Zelinsky reaction. This reaction specifically refers to the halogenation of carboxylic acids at the alpha position. **Hint**: Remember that specific reactions involving halogenation of carboxylic acids often have distinct names, like the Hell-Volhard-Zelinsky reaction. ### Final Answer The reaction is called the **Hell-Volhard-Zelinsky reaction**.
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The reaction RCH_(2)CH_(2)COOHoverset(Red P + Br_2) to R - CH_(2) - CH(Br) -COOH

CH_(3)CH=CH-CH_(3) + Br_(2) to CH_(3)-underset(Br)underset(|)(C )H-underset(Br)underset(|)(C )H-CH_(3) is an

CH_(3)CH=CH2underset(H^(+))overset(CO+H_(2)O)toCH_(3)-underset(COOH)underset(|)"CH"-CH_(2) is known as:

CH_(3)-underset(CH_(3)) underset(|) (C)= CH_(2) underset("Peroxide") overset(HBr)to CH_(3)-underset(CH_(3)) underset(|) (CH)-CH_(2)Br reaction intermediate of this reaction is:

CH_(3)CH_(2)underset(CH_(3))underset(|)(C)=CHCH_(3)overset("Reagent")toCH_(3)CH_(2)underset(CH_(3))underset(|)(CH)overset(OH)overset(|)(CH)CH_(3) Which reagent forms the above organic product as the single product in the above reaction?

'A'overset(Br_(2)+NaOH)(to)CH_(3)-underset(CH_(3))underset(|)(CH)-CH_(2)-NH_(2) Find out the Reduction Product of 'A'

Which alkyl halide from the following pairs would you expect to react more rapidly by an SN2 mechanism? Explain your answer. (i) CH_(3)CH_(2)CH_(2)CH_(2)Br or CH_(3)CH_(2)underset(Br)underset(|)C HCH_(3) , (ii) CH_(3)CH_(2)underset(Br)underset(|)CHCH_(3) or H_(3)C-underset(CH_(3))underset(|) overset(CH_(3))overset(|)C-Br (iii) CH_(3)underset(CH_(3))underset(|)CHCH_(2)CH_(2)Br or CH_(3)CH_(2)underset(CH_(3))underset(|)CHCH_(2)Br

Consider the following reactions I. II. (CH_(3))_(2) underset(OH)underset(|)(C ) - CH_(2) - CHO overset(Delta)(to) III. (CH_(3))_(2) CHCH_(2) - underset(F)underset(|)(C )H - CH_(3) underset(Delta)overset(CH_(3)O^(-)Na^(+))(to) IV. (CH_(3))_(2) CH - underset(Br)underset(|)(C )H - CH_(3) overset((CH_(3))_(3) CO^(-) k^(+))(to) Which of these reaction will not produce Hoffmann product?

Write the condensed formula and bond line formula for (a) CH_(3)-underset(CH_(3))underset(|)(CH)-CH_(2)-CH_(2)-OH (b) NH_(2)-CH_(2)-CH_(2)-CH_(2)-CH_(2)-COOH (c) CH_(3)-CH_(2)-underset(Br)underset(|)(CH)-CH_(2)-CH_(2)-CH_(3)

RESONANCE ENGLISH-CARBONYL COMPOUNDS (ALDEHYDES & KETONES ) & CARBOXYLIC ACID -Part-II
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  2. Which of the following does not undergo Hell-Volhard-Zelinsky reaction...

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  3. CH(3)CH(2)-CH(2)-COOH overset("Red P" +Br(2))toCH(3)-CH(2)-underset(B...

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  4. What product is formed when acetic acid heated with P(2)O(5)

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  5. Which of the following will not yeild a cyclic compound on heating

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  6. RCOOAg+Br(2)overset(C C1(4))underset(Delta)rarrR-Br+AgBr+CO(2) this re...

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  7. RCOOH to RCH(2)COOH. This conversion is known as reaction:

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  8. Acetic anhydride is prepared in the laboratory by heating sodium aceta...

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  9. A compound with molecular formula C(6)H(10)O(4) on acylation with acet...

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  10. How many reactions will produce carboxylic acid, as their end product

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  11. product +gas how many C^(14) atoms are present in the product

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  12. Number of possible intra molecular aldol condensation product on heati...

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  13. The reagent with which both acetaldehyde and acetophenone react easily...

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  14. How many of the following will form stable hydrate :

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  15. Which one of the following undergoes reaction with 50% sodium hydroxid...

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  16. The compound formed on heating chlorobenzene with chloral in the pres...

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  17. Reaction of cyclohexane with dimethylamine in the presence of catalyti...

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  18. CH(3)CH(2)OH overset(P+I(2))to Aunderset("ether")overset("Mg")to B ove...

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  19. In Cannizzaro reaction given below : 2PhCHO overset(: OH^(-)) to ...

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  20. Trichloroacetaldehyde was subjected to Cannizzaro's reaction by using ...

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