Skip to main content

All Questions

Tagged with
22 votes
4 answers
8k views

Why do Organolithium or Grignard reagents act as nucleophiles and not as bases with aldehydes and ketones

I've read entire Chapter 14: Organometallic Compounds of Francis Carey's "Organic Chemistry" but I still didn't get an answer to my question. Quote from the book: Because of their basicity ...
claws's user avatar
  • 963
6 votes
3 answers
3k views

Can aluminum and hydrochloric acid be used to generate hydrogen gas?

I am looking to produce hydrogen gas in a small amount with supplies I currently have. Most of the methods I have seen involve reacting zinc or magnesium with $\ce{HCl}$ to obtain the gas, but I do ...
Markovian8261's user avatar
3 votes
1 answer
785 views

Why can't Grignard reagents react like Organolithium does (with acids)?

I'd read yesterday that Grignard reagents can't give ketones on reaction with carboxylic acids. It is because of the fact that Grignard reagent is a "super-base", and it will deprotonate the ...
Rahul Verma's user avatar
  • 3,071
0 votes
0 answers
796 views

Highly concentrated NaOH solution at high temperature vs borosilicate glassware and cellulose?

I've read here on stack-exchange that NaOH will react with glass through the following reaction: 4 NaOH + SiO2 ⤑ Na4SiO4 + 2 H2O I would like to briefly heat a highly concentrated NaOH solution to ...
Hans's user avatar
  • 1,097