The reaction of 1-bromobutane with which of the following nucleophiles is a carbon chain-lengthening reaction?sodium acetylide (NaC=CH)sodium hydroxide (NaOH)O ammonia (NH3)potassium iodide (KI)

If you want to increasing the chain of carbon then you need to add extra carbon by using either CN…

Answered: The reaction of 1-bromobutar sodium…

Science

Chemistry

The reaction of 1-bromobutar sodium acetylide (NaC=C sodium hydroxide (NaOH

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter19: Aldehydes And Ketones: Nucleophilic Addition Reactions

Section19.SE: Something Extra

Problem 28VC

See similar textbooks

Related questions

Q: Estrogens are female sex hormones, the most potent of which is B-estradiol. OH AYA Но B-Estradiol In…

A: Reagents for the conversion of A to tamoxifen can be proposed as

Q: Complete the following reactions. What would you name these reactic NaBH4 a) Co 02 b) CH3-CH2-OH

A: a.The given reaction is: NaBH4 can not reduced ester group.Therefoe only ketone group reduced.…

Q: What is the role of the acetic acid in the oxidation of Cyclohexanol to Cyclohexanone? Write the…

A: Given reaction, Oxidation of cyclohexanol to cyclohexanone

Q: 104. Which of the following substances belongs to this structure? OH OH A) anthranol B) chrysacin C)…

Q: O O + H NaOH H₂O, A

A: -> In presence of base there is formation of enolate ion if carbonyl compound present which has…

Q: Write equations for the reaction of 2-butanol with reagent. Where you predict no reaction, write…

A: 2-butanol + HI ---------- > ??????

Q: Hi! I am working on some Organic Chemistry homework and one of the questions asked what would happen…

A: Butanol is an organic solvent. It behaves like non-polar solvent as the large alkyl group chain.…

Q: CH3CH2CN reacts with CH3CH2MgBr followed by acidic hydrolysis produces a(n) O 2 Penatanone O Butane…

Question

The reaction of 1-bromobutane with which of the following nucleophiles is a carbon chain-lengthening reaction?
sodium acetylide (NaC=CH)
sodium hydroxide (NaOH)
O ammonia (NH3)
potassium iodide (KI)

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

SEE SOLUTION Check out a sample Q&A here

Step 1 Carbon chain lengthening Reaction

VIEW

Step 2 Solution

VIEW

Step by step

Solved in 2 steps

SEE SOLUTION Check out a sample Q&A here

Knowledge Booster

Learn more about

Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.

Similar questions

The SN2 reaction of 1-chloropropane with which of the following nucleophiles is a carbon chain-lengthening reaction? Ammonia Potassium hydroxide Sodium cyanide Potassium iodide Sodium chloride
Which of the following sequences of reactions would convert toluene to 2-bromo-4-cyanotoluene? Bromination, nitration, reduction, diazotization, reaction with cyanide anion Bromination, nitration, diazotization, reduction , reaction with cyanide anion Nitration, bromination, reduction, diazotization, reaction with cyanide anion Nitration, bromination, diazotization, reduction, reaction with cyanide anion
help
What is the product of the reaction of ethyl bromide with each of the following nucleophiles? CH3CH2CH2O- CH3C≡C- (CH3)3N
Consider the following SN1 reaction: (CH3)3CBR + H2O → (CH3)3COH + HBr What is the effect of doubling both the t-butyl bromide and water concentrations on the rate of the reaction? O doubles the rate O quadruples the rate O triples the rate O halves the rate O no change O quarters the rate O 1/16th the rate
Draw the two reactants used to form the following compound, label the nucleophile and the electrophile, and using arrows show the points of attack of the nucleophile on the electrophile that enables the formation of the heterocyclic product.
When propene reacts with gaseous hydrogen bromide, HBr, two products, 1-bromopropane and 2-bromopropane are formed. The reaction is a two-step process in which the electrophilic attack occurs in the first step. Identify the electrophile in this reaction Draw a diagram showing the first step of the reaction that leads to the production of 2-bromopropane.
An electron-deficient carbon atom reacts with a nucleophile, symbolized as: Nu−. Define this ?
Which of the compounds listed will not undergo nucleophilic aromatic substitution? O 1-chloro-2,4-dinitrobenzene O 1-bromo-4-nitrobenzene O o-chloronitrobenzene m-chloronitrobenzene O p-chloronitrobenzene
Rank the following compounds in order of increasing reactivity in a substitution reaction with −CN as nucleophile.
Alkynes do not react directly with aqueous acid as do alkenes, but will do so in the presence of mercury(II) sulfate as a Lewis acid catalyst. The reaction occurs with Markovnikov regiochemistry, so the OH group adds to the more highly substituted carbon and the H adds to the less highly substituted carbon. The initial product of the reaction is a vinyl alcohol, also called an enol. The enol immediately rearranges to a more stable ketone via tautomerization. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions -X티 Hö: H-O -CH3 -CH3 H30*
When 2-bromo-2-methylbutane is treated with a base, a mixture of 2-methyl-2-butene and 2-methyl-1- butene is produced. When potassium hydroxide is the base, 2-methyl-1-butene accounts for 45% of the product mixture. However, when potassium tert-butoxide is the base, 2-methyl-1-butene accounts for 70% of the product mixture. What percent of 2-methyl-1-butene would be in the mixture if potassium propoxide were the base? base Br A. Less than 45% B. C. 45% Between 45% and 70% D. More than 70%