![SOLVED: 3) The intermediate alcohol, depicted in the scheme below; can be converted to its mesylate on treatment with methavesulfonvi chloride and triethylamine: Mesylates are excellent leaving groups which can be displaced SOLVED: 3) The intermediate alcohol, depicted in the scheme below; can be converted to its mesylate on treatment with methavesulfonvi chloride and triethylamine: Mesylates are excellent leaving groups which can be displaced](https://cdn.numerade.com/ask_images/828ad0298b124a84b7e729433fec7be2.jpg)
SOLVED: 3) The intermediate alcohol, depicted in the scheme below; can be converted to its mesylate on treatment with methavesulfonvi chloride and triethylamine: Mesylates are excellent leaving groups which can be displaced
![Triethylamine organic base molecule. 3D rendering. Atoms are represented as spheres with conventional color coding: hydrogen (white), carbon (grey), n Stock Photo - Alamy Triethylamine organic base molecule. 3D rendering. Atoms are represented as spheres with conventional color coding: hydrogen (white), carbon (grey), n Stock Photo - Alamy](https://c8.alamy.com/comp/R06WT9/triethylamine-organic-base-molecule-3d-rendering-atoms-are-represented-as-spheres-with-conventional-color-coding-hydrogen-white-carbon-grey-n-R06WT9.jpg)
Triethylamine organic base molecule. 3D rendering. Atoms are represented as spheres with conventional color coding: hydrogen (white), carbon (grey), n Stock Photo - Alamy
![Triethylamine Organic Base Molecule. Skeletal Formula. Stock Vector - Illustration of drawing, triethyl: 187167254 Triethylamine Organic Base Molecule. Skeletal Formula. Stock Vector - Illustration of drawing, triethyl: 187167254](https://thumbs.dreamstime.com/z/triethylamine-organic-base-molecule-skeletal-formula-187167254.jpg)
Triethylamine Organic Base Molecule. Skeletal Formula. Stock Vector - Illustration of drawing, triethyl: 187167254
![Which among the following is strongest base in gas phase? (a) Triethylamine (b) Diethylamine (c) Ethylamine (d) Ammonia Which among the following is strongest base in gas phase? (a) Triethylamine (b) Diethylamine (c) Ethylamine (d) Ammonia](https://grdp.co/cdn-cgi/image/f=auto/https://gs-post-images.grdp.co/2022/10/triethylamine-img1667201669722-23.png-rs-high-webp.png?noResize=1)
Which among the following is strongest base in gas phase? (a) Triethylamine (b) Diethylamine (c) Ethylamine (d) Ammonia
![Triethylamine: a potential N-base surrogate for pyridine in Knoevenagel condensation of aromatic aldehydes and malonic acid - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C5NJ03125G Triethylamine: a potential N-base surrogate for pyridine in Knoevenagel condensation of aromatic aldehydes and malonic acid - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C5NJ03125G](https://pubs.rsc.org/image/article/2016/NJ/c5nj03125g/c5nj03125g-s2_hi-res.gif)
Triethylamine: a potential N-base surrogate for pyridine in Knoevenagel condensation of aromatic aldehydes and malonic acid - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C5NJ03125G
![Quinuclidine and triethylamine are both tertiary amines. Quinuclidine, however, is a considerably stronger base than triethylamine. Stated alternatively, the conjugate acid of quinuclidine is a considerably weaker acid than the conjugate acid Quinuclidine and triethylamine are both tertiary amines. Quinuclidine, however, is a considerably stronger base than triethylamine. Stated alternatively, the conjugate acid of quinuclidine is a considerably weaker acid than the conjugate acid](https://homework.study.com/cimages/multimages/16/ammonia_35445692904656165184.png)
Quinuclidine and triethylamine are both tertiary amines. Quinuclidine, however, is a considerably stronger base than triethylamine. Stated alternatively, the conjugate acid of quinuclidine is a considerably weaker acid than the conjugate acid
![Triethylamine: a potential N-base surrogate for pyridine in Knoevenagel condensation of aromatic aldehydes and malonic acid - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C5NJ03125G Triethylamine: a potential N-base surrogate for pyridine in Knoevenagel condensation of aromatic aldehydes and malonic acid - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C5NJ03125G](https://pubs.rsc.org/image/article/2016/NJ/c5nj03125g/c5nj03125g-f1_hi-res.gif)